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Pepcid Complete Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet 165 mg; 10 mg; 800 mg Tablet, Chewable — NDC 66715-6422-08 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Pepcid Complete Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet 165 mg; 10 mg; 800 mg Tablet, Chewable — NDC 66715-6422-8 (Billing 66715-6422-08)

by Lil' Drug Store Products, Inc. · 30 POUCH in 1 BOX, UNIT-DOSE / 1 TABLET, CHEWABLE in 1 POUCH

This is a package of Pepcid Complete Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet 165 mg; 10 mg; 800 mg Tablet, Chewable from Lil' Drug Store Products, Inc., marketed since Apr 2022 and currently FDA-listed.

NDC 66715-6422-08
🏷️ FDA NDC (as labeled) 66715-6422-8 billing pads the package segment with a zero
This package
Contains1 tablet, chewable in 1 pouch Pack sizes2 compare ↓
Product page 66715-6422-07 Also comes in: 1 tablet 66715-6422-7
OTC Brand 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) 66715-6422-8
Product NDC 66715-6422
11-digit billing NDC 66715642208
RxCUI 283641, 688892
UNII NBZ3QY004S, H0G9379FGK, 5QZO15J2Z8
Application # NDA020958
SPL Set ID d08984b8-ce03-9e95-e053-2995a90ae6f0
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 2022-04-19
Route ORAL
Dosage form TABLET, CHEWABLE
Substance MAGNESIUM HYDROXIDE; FAMOTIDINE; CALCIUM CARBONATE
Quick answers
  • RxCUI (RxNorm): 283641
Why two NDCs? The FDA registers this code as 66715-6422-8 — a 5-4-1 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 package segment → 66715-6422-08. 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

📖 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
  • 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: 1 tablet
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
66715-6422-07 66715-6422-7 Main listing 25 POUCH in 1 BOX, UNIT-DOSE / 1 TABLET, CHEWABLE in 1 POUCH 2022-04-19 — Active
66715-6422-08 You're viewing this 30 POUCH in 1 BOX, UNIT-DOSE / 1 TABLET, CHEWABLE in 1 POUCH 2022-04-19 — Active

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 30 pouch in 1 box, unit-dose / 1 tablet, chewable in 1 pouch.
What NDC number is used to bill for this package of Pepcid Complete Famotidine, Calcium Carbonate, Magnesium Hydroxide Chewable Tablet 165 mg; 10 mg; 800 mg Tablet, Chewable?
Use the 11-digit billing form listed in the identifiers section of this page. 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 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 mgthis 66715-6422-08 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 —
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

🏛️
2022
On the market since
Apr 2022
📍
2026
Currently FDA-listed
4 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.

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.

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.

Manufacturer & labeler

LabelerLil' Drug Store Products, Inc.
Application holderKENVUE BRANDS LLC
FDA applicationNDA020958 (NDA)
Labeler code66715
First marketedApr 2022
Product typeHuman Otc Drug
Portfolio187 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 🧪 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 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 210 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)

Allergy alert: Do not use if you are allergic to famotidine or other acid reducers

🧪 Active Ingredient 17 words ▾

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

🧪 Inactive Ingredients 43 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

🎯 Purpose 5 words ▾

Purposes Acid reducer Antacid Antacid

📄 Do Not Use 34 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 66 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 23 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 8 words ▾

Questions or comments? 1-800-755-4008 (toll-free) or 215-273-8755 (collect)

📄 Package Label / Principal Display Panel ~1 min read ▾

Pepcid Complete Berry, Lil' Drug Store ® - PDP/Package DUAL ACTION Pepcid ® Complete Famotidine 10mg - Acid Reducer Calcium carbonate 800mg - Antacid Magnesium Hydroxide 165mg - Antacid Just One Tablet! Relieves Heartburn Due to Acid Indigestion Berry Flavor 2 Chewable Tablets [Lil' Drug Store logo] PDP

Pepcid ® Complete Berry, Lil' Drug Store ® - PDP/Package DUAL ACTION Pepcid® Complete Famotidine 10mg - Acid Reducer Calcium carbonate 800mg - Antacid Magnesium Hydroxide 165mg - Antacid Just One Tablet! Relieves Heartburn Due to Acid Indigestion Berry Flavor 5 Chewable Tablets [Lil' Drug Store logo] PDP

Pepcid ® Complete Berry, TRAVEL BASIX - PDP/Package DUAL ACTION Pepcid ® Complete Famotidine 10mg - Acid Reducer Calcium carbonate 800mg - Antacid Magnesium hydroxide 165mg - Antacid [image of berries & tablet] Just One Tablet! Relieves Heartburn Due to Acid Indigestion Berry Flavor 2 Chewable Tablets [TRAVEL BASIX logo] PDP/Package

Pepcid ® Complete Berry, CVP ® HEALTH - PDP/Package DUAL ACTION Pepcid ® Complete Famotidine 10mg - Acid Reducer Calcium carbonate 800mg - Antacid Magnesium hydroxide 165mg - Antacid [image of berries & tablet] Just One Tablet! Relieves Heartburn Due to Acid Indigestion Berry Flavor 2 Chewable Tablets [CVP ® HEALTH logo] PDP/Package

Pepcid ® Complete, Lil' Drug Store ® 25ct - PDP/Package DUAL ACTION Pepcid ® Complete Famotidine 10mg - Acid Reducer Calcium carbonate 800mg - Antacid Magnesium Hydroxide 165mg - Antacid Just One Tablet! Relieves Heartburn Due to Acid Indigestion Berry Flavor 25 Chewable Tablets [Lil' Drug Store logo] PDP/Package

Pepcid ® Complete, Lil Drug Store ® 30ct - PDP/Package DUAL ACTION Pepcid® Complete Famotidine 10mg - Acid Reducer Calcium carbonate 800mg - Antacid Magnesium Hydroxide 165mg - Antacid Just One Tablet! Relieves Heartburn Due to Acid Indigestion Berry Flavor 30 Chewable Tablets [Lil' Drug Store logo] PDP/Package

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) — 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

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 Lil' Drug Store Products, Inc.. 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 1 tablet (66715-6422-07). 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?
Lil' Drug Store Products, Inc. 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.
← 66715-6417-02 · Lil' 66715-6423-02 · Lil' →
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.