Home › NDC Lookup › Ingredients › Calcium Carbonate › 84126-0347-32
⚪image loading
(from DailyMed)

Rolaids POWER CHEWS 1000 Calcium carbonate 1000 mg Tablet, Chewable, 32-count

by The Procter & Gamble Manufacturing Company · 32 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (84126-347-32)
NDC 84126-0347-32
🏷️ FDA NDC (as labeled) 84126-347-32 billing pads the product 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) 84126-347-32
Product NDC 84126-347
11-digit billing NDC 84126034732
RxCUI 308892
UNII H0G9379FGK
UPC 0720112005068
Application # M001
SPL Set ID 2f9ea017-a48d-a225-e063-6294a90a9ec3
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 2025-03-04
Route ORAL
Dosage form TABLET, CHEWABLE
Substance CALCIUM CARBONATE
Why two NDCs? The FDA registers this code as 84126-347-32 — a 5-3-2 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 product segment → 84126-0347-32. 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

LabelerThe Procter & Gamble Manufacturing Company
FDA applicationM001 (OTC MONOGRAPH DRUG)
Labeler code84126
First marketedMar 2025
Product typeHuman Otc Drug
Portfolio846 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 purple
ShapeRound
ImprintRD
Size19 mm
ScoringNot scored
FlavorBerry
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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • 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 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 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 J9EQA3S2JM
    FD&C Blue No. 1 Aluminum Lake is a blue colorant made by combining FD&C Blue No. 1 dye with aluminum salts. It is used to color tablets, capsules, and other medicines for easy identification and appearance.
  • UNII 4AQJ3LG584
    A synthetic blue dye combined with aluminum to create a stable colorant. It's used in medicines and supplements to add blue color or create specific shades for product identification and appearance.
  • UNII 6T47AS764T
    Red 40 Lake is a synthetic colorant made by combining Red 40 dye with aluminum hydroxide. It's used to give tablets, capsules, and other medicines a red or pink color for identification and appearance.
  • UNII GYP6Z2JR6Q
    FD&C Yellow No. 6 Aluminum Lake is a yellow colorant made by combining FD&C Yellow No. 6 dye with aluminum salts. It's used to color tablets, capsules, and other medicines so they're easier to identify.
  • UNII JY81OXM1OM
    A plant-based oil from coconut that has been chemically treated to solidify it. It acts as a binder and filler to help hold tablet ingredients together and give the pill its shape and firmness.
  • 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 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 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 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • 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 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 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 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 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 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 7G1J5DA97F
    White wax is a refined, bleached plant-based or mineral wax that serves as a coating and hardening agent in medicines. It helps control how fast the drug dissolves and improves the product's texture and appearance.

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

The official label also statesacacia, anhydrous citric acid, caprylic/capric triglyceride, carmine, carnauba wax, corn starch, corn syrup, dextrin, FD&C Blue No. 1 Aluminum Lake, FD&C Blue No. 2 Aluminum lake, FD&C Red No. 40 Aluminum Lake, FD&C Yellow No. 6 Aluminum Lake, flavors, hydrogenated coconut oil, maltodextrin, phosphoric acid, potassium sorbate, propylene glycol, shellac, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, water, white wax

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 mg 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 mgthis 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

🏛️
2025
On the market since
Mar 2025
📍
2026
Currently FDA-listed
1 year 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
84126-0347-32 You're viewing this 32 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (84126-347-32) 2025-03-04 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 — Not published for this NDC No photo available yet for this listing.
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 84126-347-32, 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: 84126-0347-32, written without dashes as 84126034732. 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 84126-0347-32, the first segment (84126) is the labeler code FDA assigned to The Procter & Gamble Manufacturing Company; the middle segment (0347) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (32) 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 The Procter & Gamble Manufacturing Company. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
The Procter & Gamble Manufacturing Company 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 20 words ▾

Uses for the relief of: • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms

⏱️ Dosage and Administration 41 words ▾

Directions fully chew before swallowing adults and children 12 years and over: 1 chewable tablet as symptoms occur, or as directed by a doctor do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

⚠️ Warnings 121 words ▾

Warnings Ask a doctor o r 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 6 chewable tablets in a 24-period do not use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. Directions fully chew before swallowing adults and children 12 years and over: 1 chewable tablet as symptoms occur, or as directed by a doctor do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

🧪 Active Ingredient 10 words ▾

Active Ingredient (in each chewable tablet) Calcium carbonate 100 mg

🧪 Inactive Ingredients 63 words ▾

Inactive ingredients acacia, anhydrous citric acid, caprylic/capric triglyceride, carmine, carnauba wax, corn starch, corn syrup, dextrin, FD&C Blue No. 1 Aluminum Lake, FD&C Blue No. 2 Aluminum lake, FD&C Red No. 40 Aluminum Lake, FD&C Yellow No. 6 Aluminum Lake, flavors, hydrogenated coconut oil, maltodextrin, phosphoric acid, potassium sorbate, propylene glycol, shellac, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, water, white wax

🎯 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 ↗
← 84126-0346-12 · The 84126-0348-32 · The →
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.