HomeNDC LookupIngredientsCalcium Carbonate › 00135-0560-02
Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable, 6-count — NDC 00135-0560-02 package photo

Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable, 6-count

by Haleon US Holdings LLC · 6 BAR, CHEWABLE in 1 PACKAGE (0135-0560-02)
NDC 00135-0560-02
🏷️ FDA NDC (as labeled) 0135-0560-02 billing pads the labeler segment with a zero
This package
Contains6-count Pack sizes3 compare ↓
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 →
⚠️
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) 0135-0560-02
Product NDC 0135-0560
11-digit billing NDC 00135056002
NCPDP billing unit EA — each (per item)
RxCUI 1432465, 1653049
UNII H0G9379FGK
Application # M001
SPL Set ID 189850d0-6f06-45bd-bd7e-9063ee580d0b
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 2013-08-01
Route ORAL
Dosage form BAR, CHEWABLE
Substance CALCIUM CARBONATE
GPI-14 48300010000550
GPI class Tums Chewy Delights
GCN Seq No 058001
GCN 23304
HICL code 001163
Ingredient (HICL) Calcium Carbonate
HIC1 code D
Therapeutic class — broad (HIC1) Biliary System/Gastro-Intestinal System
HIC2 code D4
Therapeutic class — intermediate (HIC2) Drugs Acting Principally On The Alimentary Tract
HIC3 code D4B
Therapeutic class — specific (HIC3) Antacids
AHFS code 40:12.00.00
AHFS class Replacement Preparations
FDB label name TUMS ULTRA STR CHEWY DELIGHTS
FDB brand name Tums Ultra Strength
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 0135-0560-02 — 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 → 00135-0560-02. 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 marketedAug 2013
Product typeHuman Otc Drug
Portfolio404 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

Label name TUMS ULTRA STR CHEWY DELIGHTS Ingredient Calcium Carbonate
📖 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.

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 white / pink / orange
ShapeRectangle
Size21 mm
ScoringNot scored
FlavorOrange
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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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.
Try another pack size: 2 bars 32 bars
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
Tums Chewy Delights 1177 mgthis 00135-0560-02 Haleon 6 bars FDA listed
Tums Chewy Delights 1177 mg 00135-0561-01 Haleon 32 bars FDA listed
Tums Chewy Delights 1177 mg 00135-0569-01 Haleon 32 bars FDA listed
Antacid Soft Chew 1177 mg 00363-1081-32 Walgreen 32 tablets FDA listed
Cherry Antacid Relief Chew 1177 mg 11822-0040-01 Rite 32 tablets FDA listed
Kroger Cherry Antacid Soft Chew 1177 mg 30142-0267-32 Kroger 32 tablets FDA listed
Cherry Antacid Soft Chew 1177 mg 37808-0058-36 HEB 36 tablets FDA listed
Cherry Antacid Soft Chews 1177 mg 41250-0109-36 Meijer 36 tablets FDA listed
cherry antacid soft chew 1177 mg 41520-0031-36 American 36 tablets FDA listed
HyVee Ultra Strength Antacid Soft Chews Cherry 1177 mg 42507-0921-32 Hy-Vee 32 tablets FDA listed
Cherry Antacid Soft Chews 1177 mg 49035-0046-32 Walmart 32 tablets FDA listed
Good Sense Antacid Soft Chew 1177 mg 50804-0027-36 Geiss, 36 tablets FDA listed
Exchange Select Antacid Soft Chews Cherry Flavor 1177 mg 55301-0591-32 Army 32 tablets FDA listed
Family Wellness Antacid Relief Chews 1177 mg 55319-0049-32 Family 32 tablets FDA listed
Orange Antacid Soft Chew 1177 mg 69842-0363-36 CVS 36 tablets FDA listed
Cherry Antacid Soft Chews 1177 mg 69842-0368-36 CVS 36 tablets FDA listed
Amazon Basics Cherry Antacid SC 1177 mg 72288-0240-32 Amazon 32 tablets FDA listed
TopCare Cherry Antacid Soft Chews 1177 mg 76162-0404-32 TopCo 32 tablets FDA listed
Caring Mill Antacid 1177 mg 81522-0360-32 FSA 32 tablets FDA listed
MGC Health Antacid Soft Chews Cherry Flavor 1177 mg 83173-0130-32 Medical 32 tablets FDA listed
QC Ultra Strength Antacid Soft Chews, Cherry 1177 mg 83324-0263-32 Chain 32 tablets FDA listed
MGC Health Antacid Soft Chews Cherry Flavor 1177 mg 83698-0130-32 Xiamen 32 tablets FDA listed
QC Ultra Strength Antacid Soft Chews, Cherry 1177 mg 83698-0263-32 Xiamen 32 tablets FDA listed
Caring Mill Antacid 1177 mg 83698-0360-32 Xiamen 32 tablets FDA listed
Exchange Select Antacid Soft Chews Cherry Flavor 1177 mg 83698-0591-32 Xiamen 32 tablets FDA listed
HyVee Ultra Strength Antacid Soft Chews Cherry 1177 mg 83698-0921-32 Xiamen 32 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

🏛️
2013
On the market since
Aug 2013
📍
2026
Currently FDA-listed
13 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 Calcium carbonate — the ingredient across all brands.

Top reported reactions

Fatigue6,944
Nausea6,464
Diarrhoea5,709
Chronic Kidney Disease5,699
Pain5,437
Dyspnoea5,191
Vomiting5,014

Age at onset

Neonate89
Infant35
Child177
Adolescent182
Adult5,184
Elderly5,139

Reporter sex

73,763 reports
Male · 33%
Female · 67%
Unknown · 0%

Serious outcomes

Hospitalization29,679
Death9,717
Life-threatening6,774
Disabling5,778
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 6,672 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
00135-0560-01 32 BAR, CHEWABLE in 1 BAG (0135-0560-01) 2013-08-01 Active
00135-0560-02 You're viewing this 6 BAR, CHEWABLE in 1 PACKAGE (0135-0560-02) 2013-08-01 Active
00135-0560-03 2 BAR, CHEWABLE in 1 POUCH (0135-0560-03) 2013-08-01 Active

You're viewing one of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 00135-0560-02?
NDC 00135-0560-02 is a 6-count package — 6 bar, chewable in 1 package.
What is the difference between NDC 00135-0560-02 and NDC 00135-0560-03?
Both are Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable — the drug itself is identical. NDC 00135-0560-02 is the 6-count package, while NDC 00135-0560-03 is the 2 bars package.
What NDC number is used to bill for this package of Tums Chewy Delights calcium carbonate 1177 mg Bar, Chewable?
Bill NDC 00135-0560-02 — the 11-digit billing format is 00135056002. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 0135-0560-02, 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: 00135-0560-02, written without dashes as 00135056002. 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 00135-0560-02, the first segment (00135) is the labeler code FDA assigned to Haleon US Holdings LLC; the middle segment (0560) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 2 other package presentations of this same product, including 2 bars (00135-0560-03), 32 bars (00135-0560-01). Each has its own NDC and its own page — see the package list near the top of this page.
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 13 words

Uses Relieves: heartburn sour stomach acid indigestion upset stomach associated with these symptoms

⏱️ Dosage and Administration 41 words

Directions adults and children 12 years of age and over: chew and swallow 2-3 chews 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 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 6 chews in 24 hours if pregnant, do not take more than 4 chews 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 10 words

Active ingredient (in each chew) Calcium carbonate USP 1177 mg

🧪 Inactive Ingredients 90 words

Inactive ingredients (Smooth Peppermint) corn starch, corn syrup, corn syrup solids, FD&C blue #1, flavors, glycerin, gum arabic, hydrogenated coconut oil, non-fat dairy milk, potassium sorbate, propylene glycol, soy lecithin, sucrose

Inactive ingredients (Very Cherry) corn starch, corn syrup, corn syrup solids, FD&C red #40 lake, flavors, glycerin, hydrogenated coconut oil, non-fat dairy milk, propylene glycol, soy lecithin, sucrose

Inactive ingredients (Orange Rush) corn starch, corn syrup, corn syrup solids, FD&C yellow #6 lake, flavors, glycerin, hydrogenated coconut oil, modified food starch, non-fat dairy milk, propylene glycol, soy lecithin, sucrose

🎯 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 ↗
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.