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Signature Care Acid Reducer Complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable, 25-count — NDC 21130-0087-63 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Signature Care Acid Reducer Complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable, 25-count — NDC 21130-087-63 (Billing 21130-0087-63) · Product 21130-087

by Safeway · 25 TABLET, CHEWABLE in 1 BOTTLE (21130-087-63)

NDC 21130-087-63 (billing 21130-0087-63) is a package of 25 tablets of Signature Care Acid Reducer Complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable from Safeway, marketed since Mar 2016 and currently FDA-listed. It is the main listing for product NDC 21130-087, which comes in 2 package sizes.

NDC 21130-0087-63
🏷️ FDA NDC (as labeled) 21130-087-63 billing pads the product segment with a zero
This package
Contains25-count Pack sizes2 compare ↓
Main listing for product 21130-087 · Also comes in: 50 tablets 21130-087-71
OTC Generic On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Oct 1, 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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 21130-087-63
Product NDC 21130-087
11-digit billing NDC 21130008763
RxCUI 283641
UNII 5QZO15J2Z8, H0G9379FGK, NBZ3QY004S
Application # ANDA077355
SPL Set ID 249b19fd-d5b3-4c93-92bb-f277797015b4
Established class (EPC) Histamine-2 Receptor Antagonist
Mechanism of action Histamine H2 Receptor Antagonists
DEA schedule Non-controlled
Marketing category ANDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-03-02
Route ORAL
Dosage form TABLET, CHEWABLE
Substance FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
Quick answers for NDC 21130-087-63
  • RxCUI (RxNorm): 283641
  • 11-digit billing NDC: 21130008763
Why two NDCs? The FDA registers this code as 21130-087-63 — 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 → 21130-0087-63. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It relieves heartburn that comes with acid indigestion and sour stomach. It combines an acid reducer with antacids in one chewable tablet.
  • If you're 12 or older, chew one tablet completely when you need relief, then swallow. Don't swallow it whole. Don't take more than 2 chewable tablets in 24 hours.
  • The label says children 12 and older can use it as directed. For children under 12, ask a doctor first.
  • Stop and talk to a doctor if you need it for more than 14 days, or if your heartburn continues or gets worse. Heartburn lasting over 3 months should also be checked.
📖 Read our full Calcium Carbonate / Famotidine / Magnesium Hydroxide guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
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.

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: 50 tablets
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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
21130-0087-63 21130-087-63 You're viewing this Main listing 25 TABLET, CHEWABLE in 1 BOTTLE (21130-087-63) 2016-03-02 — Active
21130-0087-71 21130-087-71 50 TABLET, CHEWABLE in 1 BOTTLE (21130-087-71) 2016-03-02 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 21130-0087-63?
NDC 21130-0087-63 is a 25-count package — 25 tablet, chewable in 1 bottle.
What is the difference between NDC 21130-0087-63 and NDC 21130-0087-71?
Both are Signature Care Acid Reducer Complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable — the drug itself is identical. NDC 21130-0087-63 is the 25-count package, while NDC 21130-0087-71 is the 50 tablets package.
What NDC number is used to bill for this package of Signature Care Acid Reducer Complete famotidine, calcium carbonate and magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable?
Bill NDC 21130-0087-63 — the 11-digit billing format is 21130008763. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Good Sense Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 00113-0032-63 L. 25 tablets $0.258 — Availability likely —
Good Neighbor Pharmacy Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 46122-0345-63 Amerisource 25 tablets $0.258 — Availability likely —
leader acid reducer complete 10 mg/1; 800 mg/1; 165 mg 70000-0416-01 Cardinal 25 tablets $0.258 — Availability likely —
leader acid reducer complete 10 mg/1; 800 mg/1; 165 mg 70000-0582-01 Cardinal 50 tablets $0.258 — Availability likely —
foster and thrive acid reducer antacid 10 mg/1; 800 mg/1; 165 mg 70677-1100-01 Strategic 25 tablets $0.258 — Availability likely —
injoy heartburn relief 10 mg/1; 800 mg/1; 165 mg 00113-6023-63 L. 25 tablets — — FDA listed —
Good Sense Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 00113-7050-71 L. 50 tablets — — FDA listed —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 00363-0511-71 Walgreen 50 tablets — — FDA listed —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 00363-0713-33 Walgreen 60 tablets — — Discontinued —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 00363-4036-71 Walgreen 50 tablets — — FDA listed —
acid reducer plus antacid 800 mg/1; 10 mg/1; 165 mg 11822-0223-00 Rite 50 tablets — — Discontinued —
Acid Reducer Plus Antacid 10 mg/1; 165 mg/1; 800 mg 11822-0500-01 Rite 25 tablets — — Discontinued —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 16837-0246-25 Kenvue 25 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 16837-0298-12 Kenvue 100 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 16837-0891-25 Kenvue 25 tablets — — FDA listed —
Signature Care Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mgthis 21130-0087-63 Safeway 25 tablets — — FDA listed —
signature care acid reducer complete 10 mg/1; 800 mg/1; 165 mg 21130-0546-63 Safeway 25 tablets — — FDA listed —
Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 21130-0614-63 Safeway 25 tablets — — FDA listed —
acid reducer complete 10 mg/1; 800 mg/1; 165 mg 21130-0786-63 Safeway 25 tablets — — FDA listed —
DUAL ACTION Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 29485-6522-02 Lil' 1 tablet — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 30142-0040-63 Kroger 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 30142-0213-71 Kroger 50 tablets — — FDA listed —
topcare dual action complete 10 mg/1; 800 mg/1; 165 mg 36800-0082-63 Topco 25 tablets — — FDA listed —
topcare dual action complete 10 mg/1; 800 mg/1; 165 mg 36800-0616-63 Topco 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 37808-0121-63 H 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 37808-0503-63 H 25 tablets — — FDA listed —
equaline complete dual action 10 mg/1; 800 mg/1; 165 mg 41163-0321-63 United 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 41250-0284-71 Meijer 50 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 41250-0690-71 Meijer 50 tablets — — FDA listed —
CareOne Acid Reducer Complete 10 mg/1; 165 mg/1; 800 mg 41520-0409-63 American 25 tablets — — FDA listed —
CareOne Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 41520-0617-63 American 25 tablets — — FDA listed —
complete dual action 10 mg/1; 800 mg/1; 165 mg 42507-0321-50 HyVee 50 tablets — — FDA listed —
Equate Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 49035-0321-63 Wal-Mart 25 tablets — — FDA listed —
Equate Acid Reducer Complete 10 mg/1; 800 mg/1; 165 mg 49035-0546-71 Wal-Mart 50 tablets — — FDA listed —
Pepcid Complete 800 mg/1; 165 mg/1; 10 mg 50269-0016-01 JC 1 tablet — — FDA listed —
Complete Acid Reducer 10 mg/1; 800 mg/1; 165 mg 51316-0588-63 CVS 25 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 53209-4001-02 Morning 1 tablet — — FDA listed —
DG Health acid reducer complete 10 mg/1; 800 mg/1; 165 mg 55910-0808-63 Dolgencorp, 25 tablets — — FDA listed —
dual action complete 10 mg/1; 800 mg/1; 165 mg 56062-0263-63 Publix 25 tablets — — FDA listed —
Acid Reducer Plus Antacid 10 mg/1; 165 mg/1; 800 mg 59779-0738-63 CVS 25 tablets — — FDA listed —
Acid Reducer Plus Antacid 10 mg/1; 800 mg/1; 165 mg 59779-0862-63 CVS 25 tablets — — FDA listed —
Pepcid Complete 165 mg/1; 10 mg/1; 800 mg 66715-6422-07 Lil' 1 tablet — — FDA listed —
Pepcid Complete, TRAVEL BASIX 165 mg/1; 10 mg/1; 800 mg 66715-6522-02 Lil' 1 tablet — — FDA listed —
Pepcid Complete, TRAVEL BASIX 165 mg/1; 10 mg/1; 800 mg 66715-7822-02 Lil' 1 tablet — — FDA listed —
Pepcid Complete 165 mg/1; 10 mg/1; 800 mg 66715-9822-02 Lil' 1 tablet — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 67751-0202-01 Navajo 1 tablet — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 70264-0034-01 R 50 tablets — — FDA listed —
Basic Care Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 72288-0321-71 Amazon.com 50 tablets — — FDA listed —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 73097-0017-25 Savings 1 tablet — — FDA listed —
Up And Up Dual Action Acid Reducer Antacid 10 mg/1; 800 mg/1; 165 mg 82442-0321-71 Target 50 tablets — — FDA listed —
Up and Up Dual Action Acid Reducer and Antacid 10 mg/1; 800 mg/1; 165 mg 82442-0546-71 Target 50 tablets — — FDA listed —
Complete Acid Reducer 10 mg/1; 800 mg/1; 165 mg 51316-0407-63 CVS 25 tablets — — FDA listed —
Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 72288-0774-71 Amazon.com 50 tablets — — FDA listed —
About this product: this is a generic version of the medicine. FDA equivalence ratings are shown when available, and other versions are listed above, least expensive first.
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

🏛️
2016
On the market since
Mar 2016
📍
2026
Currently FDA-listed
10 years listed
🔓
·
Generic on the market
this product is a generic
✅This is a generic drug

This product is an FDA-approved generic. Other versions of the same drug are listed under Therapeutic equivalents, least expensive first.

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.

What it looks like

Color Pink
ShapeRound
ImprintL321
Size17 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 3SY5LH9PMK
    Anhydrous lactose is a milk sugar with no water content. It acts as a filler and binder in tablets and capsules, adding bulk and helping ingredients stick together.
  • UNII Z0H242BBR1
    Aspartame is an artificial sweetener made from amino acids. It's added to medicines to improve taste, making bitter or unpleasant-tasting drugs easier to take.
  • UNII ECW0LZ41X8
    A synthetic red dye used to color tablets and capsules. It helps make medicines visually distinctive so patients can easily identify their medication.
  • UNII G263MI44RU
    Dextrates are a carbohydrate mixture made from corn or potato starch. They work as fillers and binders in tablets and capsules to add bulk and help hold the medicine together.
  • 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 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 230OU9XXE4
    A waxy substance made from glycerin and stearic acid that acts as an emulsifier to blend oily and watery ingredients together. It also helps thicken and stabilize the medicine's texture.
  • UNII EWQ57Q8I5X
    Lactose monohydrate is a natural sugar derived from milk. It serves as a filler and binder in tablets and capsules, helping create the proper size, texture, and consistency of the medicine.
  • UNII 70097M6I30
    Magnesium stearate is a salt made from magnesium and stearic acid, a fatty substance. It's used in tablets and capsules as a lubricant and glidant to help ingredients flow smoothly during manufacturing and prevent sticking.
  • UNII OP1R32D61U
    Microcrystalline cellulose is a purified form of cellulose, a natural fiber from plant sources. It acts as a binder and filler in tablets and capsules, helping hold ingredients together and give the medicine its shape and size.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • 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 7SEV7J4R1U
    A powder made from a naturally occurring mineral. In medicines, talc works as a glidant and anti-caking agent, helping tablets and capsules flow smoothly during manufacturing and preventing clumping.

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

The official label also statesanhydrous lactose, artificial berry flavor, aspartame, D&C red no. 7 calcium lake, dextrates, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, glyceryl monostearate, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyacrylate dispersion, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, talc

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.

Manufacturer & labeler

LabelerSafeway
Application holderPERRIGO R AND D CO
FDA applicationANDA077355 (ANDA)
Labeler code21130
First marketedMar 2016
Product typeHuman Otc Drug
Portfolio159 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.

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 Ask a Doctor or Pharmacist Before Use If 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Use relieves heartburn associated with acid indigestion and sour stomach

⏱️ Dosage and Administration 46 words ▾

Directions • adults and children 12 years and over: • do not swallow tablet whole: chew completely • to relieve symptoms, chew 1 tablet before swallowing • do not use more than 2 chewable tablets in 24 hours • children under 12 years: ask a doctor

⚠️ Warnings 208 words ▾

Warnings Allergy alert: Do not use if you are allergic to famotidine or other acid reducers Do not use • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor. • with other acid reducers Ask a doctor before use if you have • had heartburn over 3 months.

This may be a sign of a more serious condition. • heartburn with lightheadedness, sweating, or dizziness • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness • frequent chest pain • frequent wheezing, particularly with heartburn • unexplained weight loss • nausea or vomiting • stomach pain • kidney disease Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids and acid reducers may interact with certain prescription drugs.

Stop use and ask a doctor if • your heartburn continues or worsens • you need to take this product for more than 14 days If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

(1-800-222-1222)

📦 Storage and Handling 49 words ▾

Other information • each tablet contains: calcium 330 mg; magnesium 80 mg • Phenylketonurics: Contains Phenylalanine 2 mg per tablet • read the directions and warnings before use • read the bottle. It contains important information. • store at 20-25 ° C (68-77 ° F) • protect from moisture

🧪 Active Ingredient 17 words ▾

Active ingredients (in each chewable tablet) Famotidine 10 mg Calcium carbonate 800 mg Magnesium hydroxide 165 mg

🧪 Inactive Ingredients 46 words ▾

Inactive ingredients anhydrous lactose, artificial berry flavor, aspartame, D&C red no. 7 calcium lake, dextrates, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, glyceryl monostearate, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyacrylate dispersion, polysorbate 80, povidone, pregelatinized starch, sodium starch glycolate, talc

🎯 Purpose 4 words ▾

Purposes Acid reducer Antacid

📄 Do Not Use 36 words ▾

Do not use • if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor. • with other acid reducers

📄 Ask a Doctor Before Use If 75 words ▾

Ask a doctor before use if you have • had heartburn over 3 months. This may be a sign of a more serious condition. • heartburn with lightheadedness, sweating, or dizziness • chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness • frequent chest pain • frequent wheezing, particularly with heartburn • unexplained weight loss • nausea or vomiting • stomach pain • kidney disease

📄 Ask a Doctor or Pharmacist Before Use If 24 words ▾

Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids and acid reducers may interact with certain prescription drugs.

📄 Stop Use and Ask a Doctor If 25 words ▾

Stop use and ask a doctor if • your heartburn continues or worsens • you need to take this product for more than 14 days

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

📄 Questions or Comments 4 words ▾

Questions or comments? 1-800-719-9260

📄 Package Label / Principal Display Panel 54 words ▾

Principal Display Panel Signature care ® Compare to Pepcid Complete ® active ingredients Quality Guaranteed Dual Action Acid Reducer Complete Actual Size FAMOTIDINE 10 mg CALCIUM CARBONATE 800 mg MAGNESIUM HYDROXIDE 165 mg TABLETS (CHEWABLE) Acid Reducer + Antacid Just One Tablet! Relieves heartburn due to acid indigestion BERRY Flavor 50 CHEWABLE TABLETS 321-lj-acid-reducer-complete.jpg

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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

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 21130-087-63, 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: 21130-0087-63, written without dashes as 21130008763. 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 21130-0087-63, the first segment (21130) is the labeler code FDA assigned to Safeway; the middle segment (0087) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (63) 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 Safeway. 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 1 other package presentation of this same product, including 50 tablets (21130-0087-71). 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?
Safeway 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.
← 21130-0082-26 · Safeway 21130-0088-01 · Safeway →
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.