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Tums Chewy Bites Mixed Fruit calcium carbonate 1000 mg Tablet, Chewable — NDC 00135-0641-03 package photo

Tums Chewy Bites Mixed Fruit calcium carbonate 1000 mg Tablet, Chewable

by Haleon US Holdings LLC · 3 BOTTLE in 1 PACKAGE (0135-0641-03) / 54 TABLET, CHEWABLE in 1 BOTTLE
NDC 00135-0641-03
🏷️ FDA NDC (as labeled) 0135-0641-03 billing pads the labeler segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Other active recalls for Calcium Carbonate (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0573-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0561-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0578-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0568-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0579-2026
Class II · May 28, 2026 — Presence of foreign substance: small metallic particles in chewable tablets. (Guardian Drug Co. Inc.) · FDA recall D-0560-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 0135-0641-03
Product NDC 0135-0641
11-digit billing NDC 00135064103
RxCUI 308892, 1044524
UNII H0G9379FGK
Application # M001
SPL Set ID d341b832-edcf-4cb2-96e1-c303b030c59a
Established class (EPC) Blood Coagulation Factor; Cations; Phosphate Binder
Mechanism of action Phosphate Chelating Activity
Physiologic effect Increased Coagulation Factor Activity
Chemical class Calcium; Divalent
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2021-01-15
Route ORAL
Dosage form TABLET, CHEWABLE
Substance CALCIUM CARBONATE
Why two NDCs? The FDA registers this code as 0135-0641-03 — a 4-4-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the labeler segment → 00135-0641-03. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Calcium compounds class.

Drug family (ATC) Calcium compounds, Calcium
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerHaleon US Holdings LLC
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code00135
First marketedJan 2021
Product typeHuman Otc Drug
Portfolio405 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

📖 What it is MedlinePlus · NLM

Calcium carbonate is a dietary supplement used when the amount of calcium taken in the diet is not enough. Calcium is needed by the body for healthy bones, muscles, nervous system, and heart. Calcium carbonate also is used as an antacid to relieve heartburn, acid indigestion, and upset stomach. It is available with or without a prescription. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Most people use it as a fast-acting antacid to get quick relief from heartburn, acid indigestion, sour stomach, or an upset stomach. You'll find it in brands like Tums, Rolaids, an...
  • What is calcium carbonate actually used for?
  • Don't use the maximum daily dose for more than 2 weeks in a row without talking to a doctor first. If your heartburn or stomach symptoms keep coming back or don't improve, that's y...
  • How long can I keep taking this before I should see a doctor?
📖 Read our full Calcium Carbonate guide →
4
Nutrient depletion considerations

Calcium Carbonate may be associated with lower levels of 4 nutrients — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Calcium Carbonate nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

💊 What it looks like

Color red
ShapeRound
ImprintT
Size19 mm
ScoringNot scored
FlavorCherry
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 5C5403N26O
    Acacia is a natural gum derived from acacia tree sap. It serves as a binder, thickener, and emulsifier to help hold ingredients together, improve texture, and stabilize the medicine.
  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII LMI26O6933
    Alumina is a white powder form of aluminum oxide. It's used as a filler to add bulk to tablets and capsules, and sometimes as a thickening or anti-caking agent in powdered formulations.
  • UNII 5138Q19F1X
    Ammonia is a colorless gas made from nitrogen and hydrogen. It's used in medicines as a pH buffer to maintain the correct acidity level and help keep the product stable.
  • UNII 8PJ61P6TS3
    Butyl alcohol is a clear liquid organic solvent derived from petroleum or natural sources. In medicines, it helps dissolve active ingredients and serves as a solvent in liquid formulations and some topical products.
  • UNII CID8Z8N95N
    Carminic acid is a red-to-purple dye extracted from cochineal insects. It's used in medicines as a colorant to give tablets, capsules, or liquids their red or pink appearance.
  • UNII R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII Q9L0O73W7L
    Coconut oil is a natural fat extracted from coconut fruit. It's used in medicines as a lubricant, emollient, or carrier to help dissolve or deliver active ingredients smoothly through the formulation.
  • UNII 8470G57WFM
    Corn oil is a vegetable oil extracted from corn kernels. It's used in medicines as a solvent to dissolve active ingredients and help the body absorb them, and sometimes as a lubricant in capsules.
  • UNII 9G5L16BK6N
    A thick, sweet liquid made from corn starch. It acts as a sweetener, thickener, and binder in medicines, helping create the right texture and taste while holding ingredients together.
  • UNII 76845O8NMZ
    Ethyl acetate is a clear, colorless liquid solvent derived from acetic acid and ethanol. In medicines, it dissolves active ingredients, carries them into the product formulation, and helps control how quickly the drug releases and works in your body.
  • UNII H3R47K3TBD
    FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
  • UNII L06K8R7DQK
    A synthetic blue dye approved by the FDA for use in medications and foods. It serves as a colorant to make pills and liquids visually distinct and easier to identify.
  • UNII WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • UNII H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII 2NX48Z0A9G
    Icodextrin is a glucose polymer derived from starch. It acts as a thickening agent and osmotic agent in medicines, helping to control texture and absorption in formulations like eye drops or injectable solutions.
  • UNII ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • UNII 7CVR7L4A2D
    A starch-derived carbohydrate produced by breaking down corn, potato, or tapioca starch. It functions as a filler and binder to give the medicine bulk and texture, and sometimes as a mild sweetener or texture enhancer in powders and tablets.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII 461P5CJN6T
    Modified corn starch derived from cornstarch and treated with octenyl succinic anhydride. It acts as a thickener, stabilizer, and emulsifier to improve texture and prevent separation in the medicine.
  • UNII E4GA8884NN
    Phosphoric acid is a weak mineral acid used in medicines as a buffer and pH adjuster. It helps stabilize the product and control its acidity level.
  • UNII FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII Z8IX2SC1OH
    Propylparaben is a chemical preservative used to prevent bacterial and fungal growth in medicines and personal care products. It helps extend shelf life and maintain product safety during storage.
  • UNII 46N107B71O
    Shellac is a natural resin secreted by the lac beetle. It's used as a coating on tablets and capsules to control how quickly the medicine dissolves and to improve appearance and stability.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII X045WJ989B
    Sorbic acid is a preservative derived from berries that prevents mold, yeast, and bacterial growth in medicines. It keeps the product stable and safe during storage.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • UNII O8232NY3SJ
    A plant-based carbohydrate derived from corn kernels. It acts as a filler to add bulk, a binder to hold ingredients together, and a disintegrant to help the tablet break apart in your stomach for absorption.
  • UNII C151H8M554
    A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • UNII XHX3C3X673
    Triacetin is a clear, oily liquid made from glycerin and acetic acid. It works as a plasticizer and solvent in medicines, helping soften coatings and improve how liquids mix together in formulations.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.

38 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesalcohol, ammonium hydroxide, beeswax, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, FD&C blue no. 1 aluminum lake, FD&C blue no.2 aluminum lake, FD&C red no.40, FD&C red no.40 aluminum lake, FD&C yellow no.5 aluminum lake (tartrazine), FD&C yellow no.6, FD&C yellow no.6 aluminum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, medium-chain triglycerides, methylparaben, modified starch, n-butyl alcohol, phosphoric acid, polyvinylpyrrolidone, propylene glycol, propylparaben, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, triacetin, vegetable oil

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer eachPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Leader Ultra Strength Antacid 1000 mg 70000-0436-01 CARDINAL 72 tablets $0.036 — FDA listed —
Ultra Strength Antacid Assorted Fruit 1000 mg 24385-0595-23 Amerisource 72 tablets $0.037 — Availability likely —
LEADER Ultra Strength Peppermint Flavor 1000 mg 70000-0459-01 Cardinal 72 tablets $0.037 — Availability likely —
ANTACID Ultra Strength 1000 mg 70000-0683-01 CARDINAL 72 tablets $0.037 — Availability likely —
QUALITY CHOICE Ultra Strength 1000 mg 83324-0317-72 QUALITY 72 tablets $0.037 — Availability likely —
Tums Ultra 1000 mg 00135-0118-01 Haleon 86 tablets — — FDA listed —
Tums Chewy Bites Mixed Fruit 1000 mg 00135-0138-03 Haleon 200 tablets — — Discontinued —
Tums Ultra 1000 mg 00135-0180-01 Haleon 86 tablets — — FDA listed —
Tums Ultra 1000 mg 00135-0181-01 Haleon 12 tablets — — FDA listed —
Tums Chewy Bites 1000 mg 00135-0183-01 Haleon 28 tablets — — FDA listed —
Tums Ultra 1000 mg 00135-0228-01 Haleon 12 tablets — — FDA listed —
Tums Ultra 1000 mg 00135-0235-01 Haleon 72 tablets — — FDA listed —
Tums Ultra 1000 mg 00135-0540-01 Haleon 86 tablets — — FDA listed —
Tums Ultra 1000 mg 00135-0553-01 Haleon 72 tablets — — FDA listed —
Tums Chewy Bites Mixed Fruit 1000 mgthis 00135-0641-03 Haleon 54 tablets — — FDA listed —
Tums Naturals 1000 mg 00135-1326-01 Haleon 56 tablets — — FDA listed —
Tums Naturals 1000 mg 00135-1328-01 Haleon 56 tablets — — FDA listed —
Alka-Seltzer Ultra Strength Heartburn ReliefChews Strawberry and Orange 1000 mg 00280-0059-50 Bayer 50 tablets — — FDA listed —
Alka-Seltzer Ultra Strength Heartburn ReliefChews 1000 mg 00280-0245-50 Bayer 50 tablets — — FDA listed —
Antacid Ultra Strength Assorted Fruits 1000 mg 00363-2103-72 WALGREEN 72 tablets — — FDA listed —
ULTRA STRENGTH Antacid 1000 mg 00363-2730-72 WALGREEN 72 tablets — — FDA listed —
Antacid Ultra Strength 1000 mg 00363-3113-16 WALGREEN 160 tablets — — FDA listed —
Ultra Strength Antacid Wintergreen Flavor 1000 mg 10202-0010-12 7-ELEVEN 12 tablets — — FDA listed —
Ultra Strength Antacid Tropical Fruit Flavor 1000 mg 10202-0011-12 7-ELEVEN 12 tablets — — FDA listed —
ultra strength Assorted Fruit 1000 mg 11673-0333-60 Target 160 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 11673-0776-66 TARGET 160 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 11673-0786-66 TARGET 160 tablets — — FDA listed —
ultra strength antacid Peppermint Flavored 1000 mg 11673-0813-47 Target 160 tablets — — FDA listed —
ultra strength antacid 1000 mg 11673-0933-72 Target 72 tablets — — FDA listed —
Rite Aid Ultra Strength Peppermint Flavor 1000 mg 11822-0312-07 RITE 72 tablets — — FDA listed —
Rite Aid Ultra Strength Assorted Berries 1000 mg 11822-1037-01 RITE 160 tablets — — FDA listed —
RITE AID Pharmacy Ultra Strength Assorted Fruits 1000 mg 11822-3016-00 RITE 160 tablets — — FDA listed —
Ultra Strength Antacid Peppermint 1000 mg 11822-3480-01 Rite 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Berries 1000 mg 11822-3560-01 Rite 72 tablets — — FDA listed —
Ultra Strength 1000 mg 21130-0031-72 SAFEWAY 72 tablets — — FDA listed —
Ultra Strength 1000 mg 21130-0302-60 BETTER 160 tablets — — FDA listed —
Ultra Strength 1000 mg 21130-0310-60 BETTER 160 tablets — — FDA listed —
Antacid Relief 1000 mg 21130-0472-68 Safeway 72 tablets — — FDA listed —
Ultra Strength Natural Antacid 1000 mg 30142-0108-72 KROGER 72 tablets — — FDA listed —
Kroger Ultra Strength Assorted Berry 1000 mg 30142-0300-16 KROGER 160 tablets — — FDA listed —
Kroger Ultra Strength Assorted Fruit 1000 mg 30142-0307-72 KROGER 72 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 30142-0993-16 THE 160 tablets — — FDA listed —
topcare Antacid Calcium Ultra Strength 1000 mg 36800-0595-24 Topco 72 tablets — — FDA listed —
Topcare Antacid Calcium 1000 mg 36800-0881-24 Topco 72 tablets — — FDA listed —
Topcare antacid calcium 1000 mg 36800-0962-25 Topco 72 tablets — — FDA listed —
HEB Antacid Calcium Assorted Berry 1000 mg 37808-0103-14 HEB 72 tablets — — FDA listed —
HEB Ultra Strength Assorted Fruits 1000 mg 37808-0203-17 HEB 160 tablets — — FDA listed —
Bi-Mart Ultra Strength Antacid Assorted Fruit 1000 mg 37835-0171-75 Bi-Mart 160 tablets — — FDA listed —
BI-MART Ultra Strength Antacid Peppermint 1000 mg 37835-0471-75 Bi-Mart 160 tablets — — FDA listed —
EQU Ultra Strength Antacid Assorted Fruit 171AF 1000 mg 41163-0171-68 UNITED 72 tablets — — FDA listed —
Equaline Ultra Strength Antacid Assorted Berry Ultra strength Assorted Fruit Antacid 1000 mg 41163-0184-68 UNITED 72 tablets — — FDA listed —
Meijer Ultra Strength Antacid Assorted Fruit 1000 mg 41250-0420-72 MEIJER 72 tablets — — FDA listed —
Antacid 1000 mg 41250-0723-72 Meijer 72 tablets — — FDA listed —
Publix Ultra Strength Assorted Fruit 1000 mg 41415-0103-72 PUBLIX 72 tablets — — FDA listed —
Ultra Strength Assorted Berry Antacid 1000 mg 42507-0171-68 Hyvee 72 tablets — — FDA listed —
Ultra Strength Assorted Fruit Antacid 1000 mg 42507-0709-68 Hyvee 72 tablets — — FDA listed —
WHOLE FOODS MARKET Health Ultra Strength Natural Antacid Peppermint Flavor 1000 mg 42681-0004-01 WHOLE 160 tablets — — FDA listed —
equate Ultra Strength Antacid Peppermint Flavor 1000 mg 49035-0101-47 Wal-Mart 160 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 49035-0167-16 Wal-Mart 160 tablets — — FDA listed —
Equate Ultra Stregth Antacid 1000 mg 49035-0778-80 Wal-Mart 265 tablets — — FDA listed —
Ultra Strength Antacid Assorted Berries 1000 mg 49035-0803-16 WAL-MART 160 tablets — — FDA listed —
GOODSENSE Ultra Strength Antacid Assorted Fruit 1000 mg 50804-0171-68 GoodSense 72 tablets — — FDA listed —
Goodsense Ultra Strength Antacid 1000 mg 50804-0175-68 Good 72 tablets — — FDA listed —
GOODSENSE Ultra Strength Antacid Peppermint 1000 mg 50804-0176-68 GoodSense 72 tablets — — FDA listed —
CVS Tropical Fruit 1000 mg 51316-0003-60 CVS 160 tablets — — FDA listed —
CVS Ultra Strength 1000 mg 51316-0031-72 CVS 72 tablets — — FDA listed —
CVS PHARMACY Assorted Fruit Antacid 1000 mg 51316-0103-60 CVS 160 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 51316-0171-68 CVS 72 tablets — — FDA listed —
CVS Naturals 1000 mg 51316-0300-56 CVS 56 tablets — — FDA listed —
CVS PHARMACY Assorted Berry Antacid 1000 mg 51316-0301-60 CVS 160 tablets — — FDA listed —
Maximum Strength Calcium Carbonate 1000mg 1000 mg 51316-0540-66 CVS 160 tablets — — FDA listed —
Calcium Carbonate 1000 mg 51316-0639-66 CVS 160 tablets — — FDA listed —
Ultra strength Antacid 1000 mg 51316-0905-66 CVS 160 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 51316-0908-75 CVS 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Berries 1000 mg 53041-0161-68 Guardian 72 tablets — — FDA listed —
Guardian Ultra Strength Antacid Assorted Fruit 1000 mg 53041-0171-68 Guardian 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Fruit 1000 mg 53942-0171-68 DeMoulas 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Fruit 1000 mg 53943-0171-68 Discount 72 tablets — — FDA listed —
exchange select Ultra Strength Antacid Assorted Fruit 1000 mg 55301-0203-13 ARMY 72 tablets — — FDA listed —
Family Wellness Ultra Strength Assorted Fruit Antacid Ultra strength Assorted Fruit Antacid 1000 mg 55319-0171-68 Family 72 tablets — — FDA listed —
Family Wellness Ultra Stregth Antacid 171AB 1000 mg 55319-0919-68 Family 72 tablets — — FDA listed —
DG HEALTH Ultra Strength 1000 mg 55910-0083-50 DOLGENCORP, 72 tablets — — FDA listed —
DG health Ultra Strength Assorted Fruit Antacid 1000 mg 55910-0273-72 DOLGENCORP, 72 tablets — — FDA listed —
DG health Ultra Strength Assorted Berry Antacid 1000 mg 55910-0315-72 DOLGENCORP, 72 tablets — — FDA listed —
CVS Health Ultra Strength Natural Antacid Peppermint Flavor 1000 mg 59779-0675-72 CVS 72 tablets — — FDA listed —
Quality Choice Ultra Strength Assorted Fruit 1000 mg 63868-0048-72 CHAIN 72 tablets — — FDA listed —
QC Antacid Calcium Assorted Berry 1000 mg 63868-0049-72 CHAIN 72 tablets — — FDA listed —
Best Choice Ultra Strength 1000 mg 63941-0031-16 BEST 160 tablets — — FDA listed —
Kirkland Ultra Stregth Antacid 171AB 1000 mg 63981-0171-80 COSTCO 265 tablets — — FDA listed —
WinCo FOODS Antacid Ultra Strength 1000 mg 67091-0358-72 WINCO 72 tablets — — FDA listed —
WinCo FOODS Antacid Ultra Strength 1000 mg 67091-0365-72 WINCO 72 tablets — — FDA listed —
Ultra Strength Assorted Berries 1000 mg 68196-0103-65 SAM'S 265 tablets — — FDA listed —
Berkley Jensen Ultra Strength 1000 mg 68391-0033-65 BJWC 265 tablets — — FDA listed —
Marc Glassman Ultra Strength 1000 mg 68998-0103-72 MARC 72 tablets — — FDA listed —
Ultra Strength Assorted Berry Antacid 1000 mg 69256-0171-68 Harris 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Fruit 1000 mg 69256-0178-68 Harris 72 tablets — — FDA listed —
Genexa Antacid Maximum Strength 1000 mg 69676-0072-04 Genexa 72 tablets — — FDA listed —
Genexa Antacid Maximum Strength 1000 mg 69676-0098-04 Genexa 72 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 69842-0171-68 CVS 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Berries 1000 mg 69842-0271-68 CVS 72 tablets — — FDA listed —
Ultra Strength Antacid Tropical fruit 1000 mg 69842-0371-68 CVS 72 tablets — — FDA listed —
Lidl Ultra Strength Antacid Calcium Carbonate Assorted Fruit 1000 mg 71141-0144-32 Lidl 72 tablets — — FDA listed —
AMAZON Ultra Strength Tropical Fruit 1000 mg 72288-0106-60 AMAZON.COM 160 tablets — — FDA listed —
Amazon Ultra Strength Antacid 1000 mg 72288-0504-60 AMAZON.COM 160 tablets — — FDA listed —
Ultra Strength Antacid Assorted Fruit 1000 mg 72476-0170-23 Retail 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Berries 1000 mg 72476-0178-23 Retail 72 tablets — — FDA listed —
TopCare Ultra Strength Antacid Assorted Fruit 1000 mg 76162-0129-68 Topco 72 tablets — — FDA listed —
TopCare Ultra Strength Antacid Assorted Berry 1000 mg 76162-0130-68 Topco 72 tablets — — FDA listed —
Topcare Ultra Strength Antacid Peppermint 1000 mg 76162-0131-68 Topco 72 tablets — — FDA listed —
Ultra Strength Antacid Assorted Fruit 1000 mg 79903-0103-72 Wal-Mart 72 tablets — — FDA listed —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0101-03 Ginger 3 tablets — — Discontinued —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0102-03 Ginger 3 tablets — — Discontinued —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0103-03 Ginger 3 tablets — — Discontinued —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0104-03 Ginger 3 tablets — — Discontinued —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0105-03 Ginger 3 tablets — — Discontinued —
Wonderbelly Maximum Strength Antacid - Sweet Mint 1000 mg 82431-0106-12 Ginger 12 tablets — — FDA listed —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0107-60 Ginger 60 tablets — — FDA listed —
Wonderbelly Maximum Strength Antacid 1000 mg 82431-0108-12 Ginger 12 tablets — — Discontinued —
Wonderbelly Maximum Strength Antacid 82431-0191-12 Ginger 12 tablets — — Discontinued —
FEVIA Acid Control 1000 mg 82706-0027-02 VIVUNT 60 tablets — — FDA listed —
MGC Health Calcium Carbonate Antacid Assorted Fruits 1000 mg 83173-0136-16 Medical 160 tablets — — FDA listed —
MGC Health Calcium Carbonate Antacid Assorted Berries 1000 mg 83173-0137-16 Medical 160 tablets — — FDA listed —
MGC Health Calcium Carbonate Antacid Tropical Fruit 1000 mg 83173-0138-16 Medical 160 tablets — — FDA listed —
Quality Choice Ultra Strength 1000 mg 83324-0314-72 QUALITY 72 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 83455-0171-68 UNITED 72 tablets — — FDA listed —
Ultra Strength Antacid Wintergreen Flavor 1000 mg 83698-0010-12 Xiamen 12 tablets — — FDA listed —
Ultra Strength Antacid Tropical Fruit Flavor 1000 mg 83698-0011-12 Xiamen 12 tablets — — FDA listed —
MGC Health Calcium Carbonate Antacid Assorted Fruits 1000 mg 83698-0136-16 Xiamen 160 tablets — — FDA listed —
MGC Health Calcium Carbonate Antacid Assorted Berries 1000 mg 83698-0137-16 Xiamen 160 tablets — — FDA listed —
MGC Health Calcium Carbonate Antacid Tropical Fruit 1000 mg 83698-0138-16 Xiamen 160 tablets — — FDA listed —
Rolaids POWER CHEWS 1000 1000 mg 84126-0347-32 The 32 tablets — — FDA listed —
Rolaids POWER CHEWS 1000 1000 mg 84126-0348-32 The 32 tablets — — FDA listed —
Genexa Antacid Maximum Strength 1000 mg 84998-0098-04 PNP 72 tablets — — FDA listed —
Ultra Strength Antacid 1000 mg 85828-0905-75 Grocery 72 tablets — — FDA listed —
Antacid- Calcium Carbonate 1000 mg 87745-0001-01 Anhui 12 tablets — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2021
On the market since
Jan 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Tums Chewy Bites Mixed Fruit (this brand).

Top reported reactions

Fatigue4,865
Nausea4,279
Pain4,067
Dyspnoea3,877
Diarrhoea3,722
Vomiting3,650
Pneumonia3,264

Age at onset

Neonate80
Infant20
Child108
Adolescent139
Adult3,532
Elderly3,645

Reporter sex

46,845 reports
Male · 32%
Female · 68%
Unknown · 0%

Serious outcomes

Hospitalization22,384
Death7,136
Life-threatening5,526
Disabling4,062
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 3,348 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
00135-0641-03 You're viewing this 3 BOTTLE in 1 PACKAGE (0135-0641-03) / 54 TABLET, CHEWABLE in 1 BOTTLE 2021-01-15 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 0135-0641-03, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 00135-0641-03, written without dashes as 00135064103. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 00135-0641-03, the first segment (00135) is the labeler code FDA assigned to Haleon US Holdings LLC; the middle segment (0641) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (03) identifies this exact package size and type. Together they name one specific package of one specific product.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Haleon US Holdings LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Haleon US Holdings LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 13 words ▾

Uses relieves heartburn acid indigestion sour stomach upset stomach associated with these symptoms

⏱️ Dosage and Administration 46 words ▾

Directions adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing. do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

⚠️ Warnings 75 words ▾

Warnings Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product do not take more than 4 tablets in 24 hours if pregnant do not take more than 4 tablets in 24 hours do not use the maximum dosage for more than 2 weeks except, under the advice and supervision of a doctor Keep out of reach of children.

🧪 Active Ingredient 5 words ▾

Active ingredient Calcium carbonate 1000mg

🧪 Inactive Ingredients 88 words ▾

Inactive ingredients alcohol, ammonium hydroxide, beeswax, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, FD&C blue no. 1 aluminum lake, FD&C blue no.2 aluminum lake, FD&C red no.40, FD&C red no.40 aluminum lake, FD&C yellow no.5 aluminum lake (tartrazine), FD&C yellow no.6, FD&C yellow no.6 aluminum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, medium-chain triglycerides, methylparaben, modified starch, n-butyl alcohol, phosphoric acid, polyvinylpyrrolidone, propylene glycol, propylparaben, purified water, shellac, sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, triacetin, vegetable oil

🎯 Purpose 2 words ▾

Purpose Antacid

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 00135-0638-03 · Haleon 00135-0642-01 · Haleon →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.