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Pepcid Complete Famotidine, Calcium carbonate, and Magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable — NDC 16837-0298-68 package photo

Pepcid Complete Famotidine, Calcium carbonate, and Magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable

by Kenvue Brands LLC · 8 POUCH in 1 CARTON (16837-298-68) / 1 TABLET, CHEWABLE in 1 POUCH
NDC 16837-0298-68
🏷️ FDA NDC (as labeled) 16837-298-68 billing pads the product segment with a zero
This package
Contains1 tablet, chewable in 1 pouch Pack sizes9 compare ↓
Also comes in: 1 tablet 16837-0298-65 1 tablet 16837-0298-67 1 tablet 16837-0298-52 25 tablets 16837-0298-25 50 tablets 16837-0298-50 70 tablets 16837-0298-70 72 tablets 16837-0298-72 100 tablets 16837-0298-12
OTC Brand On market Non-controlled
🗂️ Data synced Aug 27, 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

FDA NDC (as labeled) 16837-298-68
Product NDC 16837-298
11-digit billing NDC 16837029868
RxCUI 283641, 688892
UNII 5QZO15J2Z8, H0G9379FGK, NBZ3QY004S
UPC 0716837291251
Application # NDA020958
SPL Set ID e874118f-b4fe-4c80-aece-99ea20e7e805
Established class (EPC) Histamine-2 Receptor Antagonist
Mechanism of action Histamine H2 Receptor Antagonists
DEA schedule Non-controlled
Marketing category NDA
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2009-03-01
Route ORAL
Dosage form TABLET, CHEWABLE
Substance FAMOTIDINE; CALCIUM CARBONATE; MAGNESIUM HYDROXIDE
GCN Seq No 047669
GCN 13069
HICL code 021332
Ingredient (HICL) Famotidine/Ca Carb/Mag Hydrox
HIC1 code Z
Therapeutic class — broad (HIC1) Body As A Whole
HIC2 code Z2
Therapeutic class — intermediate (HIC2) Antihistamines, Antiserotonins, Immunosuppressants
HIC3 code Z2D
Therapeutic class — specific (HIC3) Histamine H2-Receptor Inhibitors
AHFS code 04:92.00.00
AHFS class Other Antihistamines
FDB label name PEPCID COMPLETE TABLET CHEW
FDB brand name Pepcid Complete
Legend status O — Over-the-counter (OTC) drug or device
Why two NDCs? The FDA registers this code as 16837-298-68 — 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 → 16837-0298-68. 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

LabelerKenvue Brands LLC
Application holderKENVUE BRANDS LLC
FDA applicationNDA020958 (NDA)
Labeler code16837
First marketedMar 2009
Product typeHuman Otc Drug
Portfolio564 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 PEPCID COMPLETE TABLET CHEW Ingredient Famotidine/Ca Carb/Mag Hydrox
📗 Our plain-language guide HelloPharmacist
  • This tablet combines two antacids — calcium carbonate and magnesium hydroxide — with famotidine, an acid reducer. The antacids work quickly to neutralize acid that's already in you...
  • What exactly does this tablet do — how is it different from a regular antacid?
  • You do need to chew it completely before swallowing — that's important. Don't swallow the tablet whole. Chewing it first is part of how it works and how it's meant to be used safel...
  • Do I have to chew it, or can I just swallow it?
📖 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.

💊 What it looks like

Color purple
ShapeRound
ImprintP
Size18 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 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 3J2P07GVB6
    Cellulose acetate is a plant-derived polymer made by chemically modifying cellulose fibers. In medications, it serves as a film-coating material for tablets and capsules to protect the drug, control release, and improve appearance.
  • UNII 2S7830E561
    Crospovidone is a synthetic polymer derived from povidone. It acts as a disintegrant, helping the tablet or capsule break apart quickly in the stomach so the active ingredient can be absorbed.
  • 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 IY9XDZ35W2
    Dextrose is a simple sugar derived from corn or other sources. It serves as a filler and sweetener in medicines to add bulk, improve taste, and help stabilize the medication's form.
  • 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 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 9XZ8H6N6OH
    A plant-based cellulose derivative used as a binder to hold tablet ingredients together, a thickener in liquids, and a coating agent to control how fast the medicine dissolves.
  • UNII 3NXW29V3WO
    Hypromellose is a plant-based thickener made from cellulose. It's used in medicines as a binder to hold ingredients together, a coating for tablets, and a thickener for liquids.
  • 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 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 T5L8T28FGP
    Mineral oil is a clear, odorless liquid derived from crude oil. It acts as a lubricant and emollient in medications, helping pills slide smoothly during manufacturing and aiding moisture retention in topical products.
  • 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 96K6UQ3ZD4
    Sucralose is a synthetic sweetener made from sugar. It's added to medicines to improve taste without adding calories, helping make bitter or unpleasant-tasting drugs easier to take.

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

The official label also statescellulose acetate, corn starch, crospovidone, D&C red no. 7 calcium lake, dextrose excipient, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, flavors, gum arabic, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, maltodextrin, mineral oil*, modified starch, sucralose *may contain mineral 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.
Try another pack size: 1 tablet 1 tablet 1 tablet 25 tablets 50 tablets 70 tablets 72 tablets 100 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.

🔁 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 $0.261 — Availability likely —
Good Neighbor Pharmacy Dual Action Complete 10 mg/1; 800 mg/1; 165 mg 46122-0345-63 Amerisource 25 tablets $0.261 — Availability likely —
leader acid reducer complete 10 mg/1; 800 mg/1; 165 mg 70000-0416-01 Cardinal 25 tablets $0.261 — Availability likely —
leader acid reducer complete 10 mg/1; 800 mg/1; 165 mg 70000-0582-01 Cardinal 50 tablets $0.261 — Availability likely —
foster and thrive acid reducer antacid 10 mg/1; 800 mg/1; 165 mg 70677-1100-01 Strategic 25 tablets $0.261 — 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 — — FDA listed —
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 mgthis 16837-0298-68 Kenvue 1 tablet — — 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 mg 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 —
Pepcid Complete 10 mg/1; 800 mg/1; 165 mg 85237-1948-01 Select 1 tablet — — FDA listed —
About this product: this is the brand-name version. Some generic versions are approved by the FDA, but we could not confirm current pharmacy availability from our pricing/market data.
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

🏛️
2009
On the market since
Mar 2009
📍
2026
Currently FDA-listed
17 years listed
🔒
·
Generic approved (availability unconfirmed)
see note
🔒Generic approved by FDA, but pharmacy availability is not confirmed

The FDA lists approved generic versions of this medicine, but that does not always mean a pharmacy can get one today. Patent rules, launch agreements, supply and pricing can affect when generics actually arrive.

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 Pepcid Complete (this brand).

Top reported reactions

Chronic Kidney Disease483
Acute Kidney Injury257
Renal Failure174
End Stage Renal Disease133
Gastrooesophageal Reflux Disease133
Therapeutic Response Unexpected92
Dysgeusia78

Age at onset

Infant12
Child36
Adolescent3
Adult333
Elderly227

Reporter sex

0 reports
Male · 34%
Female · 66%

Serious outcomes

Hospitalization116
Death74
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 334 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
16837-0298-12 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16837-298-12) 2009-03-01 Active
16837-0298-25 25 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16837-298-25) 2009-03-01 Active
16837-0298-50 50 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16837-298-50) 2009-03-01 Active
16837-0298-65 2500 POUCH in 1 CARTON (16837-298-65) / 1 TABLET, CHEWABLE in 1 POUCH 2020-06-15 Active
16837-0298-67 4 POUCH in 1 CARTON (16837-298-67) / 1 TABLET, CHEWABLE in 1 POUCH 2020-06-15 Active
16837-0298-68 You're viewing this 8 POUCH in 1 CARTON (16837-298-68) / 1 TABLET, CHEWABLE in 1 POUCH 2020-06-15 Active
16837-0298-52 50 POUCH in 1 CARTON (16837-298-52) / 1 TABLET, CHEWABLE in 1 POUCH 2025-10-31 Active
16837-0298-70 70 TABLET, CHEWABLE in 1 BOTTLE (16837-298-70) 2025-08-29 Active
16837-0298-72 72 TABLET, CHEWABLE in 1 BOTTLE (16837-298-72) 2026-05-29 Active

Pack size FAQ

What quantity is in NDC 16837-0298-68?
NDC 16837-0298-68 is listed by the FDA — 8 pouch in 1 carton / 1 tablet, chewable in 1 pouch.
What NDC number is used to bill for this package of Pepcid Complete Famotidine, Calcium carbonate, and Magnesium hydroxide 10 mg; 800 mg; 165 mg Tablet, Chewable?
Bill NDC 16837-0298-68 — the 11-digit billing format is 16837029868. 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) ✓ 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 16837-298-68, 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: 16837-0298-68, written without dashes as 16837029868. 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 16837-0298-68, the first segment (16837) is the labeler code FDA assigned to Kenvue Brands LLC; the middle segment (0298) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (68) 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 Kenvue Brands 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 8 other package presentations of this same product, including 1 tablet (16837-0298-65), 1 tablet (16837-0298-67), 1 tablet (16837-0298-52). 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?
Kenvue Brands 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 10 words ▾

Use relieves heartburn associated with acid indigestion and sour stomach

⏱️ Dosage and Administration 41 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 195 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 320 mg, magnesium 70 mg 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 do not use if foil inner seal imprinted with "Sealed For Your Safety" is broken or missing

🧪 Active Ingredient 22 words ▾

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

🧪 Inactive Ingredients 47 words ▾

Inactive ingredients cellulose acetate, corn starch, crospovidone, D&C red no. 7 calcium lake, dextrose excipient, FD&C blue no. 1 aluminum lake, FD&C red no. 40 aluminum lake, flavors, gum arabic, hydroxypropyl cellulose, hypromellose, lactose monohydrate, magnesium stearate, maltodextrin, mineral oil*, modified starch, sucralose *may contain mineral oil

🎯 Purpose 22 words ▾

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

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 16837-0246-25 · Kenvue 16837-0839-00 · Kenvue →
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.