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Mylanta Gas Minis Assorted Fruit Flavor Simethicone 125 mg Tablet, Chewable, 60-count — NDC 62372-0801-60 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Mylanta Gas Minis Assorted Fruit Flavor Simethicone 125 mg Tablet, Chewable, 60-count — NDC 62372-801-60 (Billing 62372-0801-60)

by Infirst Healthcare Inc. · 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC

This is a package of 60 tablets of Mylanta Gas Minis Assorted Fruit Flavor Simethicone 125 mg Tablet, Chewable from Infirst Healthcare Inc., marketed since Mar 2016 and currently FDA-listed.

NDC 62372-0801-60
🏷️ FDA NDC (as labeled) 62372-801-60 billing pads the product segment with a zero
This package
Contains60-count Pack sizes3 compare ↓
Product page 62372-0801-03 Also comes in: 3 tablets 62372-801-03 50 tablets 62372-801-50
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

NDC database record

One package, one record: these facts belong to NDC 62372-801-60 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
62372 labeler · 801 product · 60 package
Package marketed since
Mar 21, 2016
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0819903010371
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 62372-801-60
Product NDC 62372-801
11-digit billing NDC 62372080160
RxCUI 314221
UNII 92RU3N3Y1O
UPC 0819903010371
Application # M002
SPL Set ID c6db9af2-d457-477d-baa9-470ddbba5905
Physiologic effect Skin Barrier Activity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-03-21
Route ORAL
Dosage form TABLET, CHEWABLE
Substance DIMETHICONE
Quick answers
  • RxCUI (RxNorm): 314221
Why two NDCs? The FDA registers this code as 62372-801-60 — 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 → 62372-0801-60. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It relieves the discomfort of gas. For adults, that means pressure, bloating and fullness. Infant drops are for baby gas, often caused by swallowed air or certain formulas or foods...
  • Shake the bottle well. Use only the syringe or dropper that came with it. Dispense it slowly toward the inner cheek. You can also mix it with 1 oz. of cool water, formula or anothe...
  • Doses can be repeated as needed after meals and at bedtime. Do not go over 12 doses in a day. Follow your product’s label and your doctor’s advice.
  • If you can, use your child’s weight. If not, use age. Check the chart on your product, and ask me or your doctor if you are unsure.
📖 Read our full Simethicone guide →
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: 3 tablets 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
62372-0801-03 62372-801-03 Main listing 3 TABLET, CHEWABLE in 1 POUCH 2019-10-04 — Discontinued by firm
62372-0801-50 62372-801-50 50 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC 2016-03-21 — Discontinued by firm
62372-0801-60 You're viewing this 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC 2016-03-21 — Active

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

Pack size FAQ

What quantity is in this package?
This is a 60-count package — 60 tablet, chewable in 1 bottle, plastic.
How does this package differ from NDC 62372-0801-03?
Both are Mylanta Gas Minis Assorted Fruit Flavor Simethicone 125 mg Tablet, Chewable — the drug itself is identical. This page's package is the 60-count one, while NDC 62372-0801-03 is the 3 tablets package.
What NDC number is used to bill for this package of Mylanta Gas Minis Assorted Fruit Flavor Simethicone 125 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
gas relief 125 mg 62011-0189-01 Strategic 9 tablets $0.097 — FDA listed —
Rugby Gas relief 125 mg 00536-1223-08 Rugby 60 tablets $0.103 — Availability likely —
extra strength Gas Relief cherry creme 125 mg 46122-0811-08 Amerisource 9 tablets $0.103 — Availability likely —
Foster and Thrive Extra Strength Gas Relief Cherry 125 mg 70677-1077-01 Strategic 9 tablets $0.103 — Availability likely —
Gas-X Extra Strength 125 mg 00067-0117-01 Haleon 12 tablets — — FDA listed —
Gas-X Extra Strength 125 mg 00067-0129-18 Haleon 9 tablets — — FDA listed —
Walgreens Extra Strength 125 mg 00363-0118-18 WALGREENS 9 tablets — — FDA listed —
Extra Strength Gas Relief 125 mg 00363-0119-18 WALGREENS 9 tablets — — FDA listed —
Gas Relief - Cherry Flavor 125 mg 11673-0066-48 TARGET 12 tablets — — FDA listed —
up and up extra strength gas relief chewables Extra Strength 125 mg 11673-0610-48 Target 12 tablets — — FDA listed —
Gas Relief 125 mg 11822-6080-02 Rite 12 tablets — — FDA listed —
Simethicone 125 mg 17714-0040-60 Advance 60 tablets — — FDA listed —
Simethicone 125 mg 17856-0137-01 ATLANTIC 1 tablet — — FDA listed —
Extra Strength Gas Relief 125 mg 21130-0110-18 SAFEWAY 6 tablets — — FDA listed —
Gas Relief 125 mg 21130-0135-73 Safeway 9 tablets — — FDA listed —
Extra Strength Gas Relief 125 mg 21130-0441-18 SAFEWAY 9 tablets — — FDA listed —
Kroger Extra Strength Gas Relief 125 mg 30142-0481-48 KROGER 4 tablets — — FDA listed —
Gas Relief 125 mg 36800-0122-73 Topco 6 tablets — — FDA listed —
TopCare Extra Strength Gas Relief Cherry Creme 125 mg 36800-0488-48 TOPCO 48 tablets — — FDA listed —
HEB Gas Relief Extra Strength Peppermint 125 mg 37808-0155-73 H 9 tablets — — FDA listed —
Extra Strength Gas Relief Cherry 125 mg 37808-0692-13 H 12 tablets — — FDA listed —
Extra Strength Simethicone 125 mg 37835-0233-18 Bi-Mart 9 tablets — — FDA listed —
gas relief 125 mg 41163-0408-44 United 9 tablets — — FDA listed —
Extra Strength gas relief 125 mg 41415-0110-18 PUBLIX 6 tablets — — FDA listed —
Extra Strength Gas Relief 125 mg 42507-0701-34 Hyvee 9 tablets — — FDA listed —
Extra Strength Gas Relief 125 mg 49035-0910-48 Wal-Mart 48 tablets — — FDA listed —
Extra Strength Gas Relief Cherry 125 mg 50804-0134-73 Good 9 tablets — — FDA listed —
CVS PHARMACY Extra Strength Gas Relief 125 mg 51316-0011-18 CVS 9 tablets — — FDA listed —
CVS PHARMACY Extra Strength 125 mg 51316-0110-18 CVS 9 tablets — — FDA listed —
Extra Strength Gas Relief Cherry Creme 125 mg 51316-0134-13 CVS 9 tablets — — FDA listed —
Extra Strength Gas Relief Cherry Flavor 125 mg 53943-0134-39 Discount 9 tablets — — FDA listed —
Gas Relief Extra Strength 125 mg 55301-0680-44 ARMY 9 tablets — — FDA listed —
Family Wellness Extra Strength Gas Relief Cherry 125 mg 55319-0134-34 Family 12 tablets — — FDA listed —
Extra Strength Gas Relief 125 mg 57896-0694-03 Geri-Care 30 tablets — — FDA listed —
Mylanta Gas Minis Mint Flavor 125 mg 62372-0800-50 Infirst 50 tablets — — FDA listed —
Mylanta Gas Minis Assorted Fruit Flavor 125 mgthis 62372-0801-60 Infirst 60 tablets — — FDA listed —
Best Choice Extra Strength 125 mg 63941-0110-18 BEST 9 tablets — — FDA listed —
WinCo FOODS Extra Strength Gas Relief 125 mg 67091-0361-18 WINCO 6 tablets — — FDA listed —
Premier Value Extra Strength 125 mg 68016-0811-18 PHARMACY 9 tablets — — FDA listed —
Extra Strength Gas Relief Cherry 125 mg 69256-0134-73 Harris 9 tablets — — FDA listed —
Extra Strength Gas Relief 125 mg 69256-0135-73 Harris 9 tablets — — FDA listed —
Simethicone 125 mg 69618-0032-06 Reliable 60 tablets — — FDA listed —
Gas-Aid 125 mg 69626-7197-03 Leosons 9 tablets — — FDA listed —
Firstcare Gas Relief Simethicone 125 mg Anti-gas 71594-0709-10 USpharma 100 tablets — — FDA listed —
Extra Strength Gas Relief Cherry 125 mg 72476-0134-73 Retail 9 tablets — — FDA listed —
Gas Relief 125 mg 79481-0608-04 Meijer 9 tablets — — FDA listed —
Gas Relief 125 mg 80136-0859-68 Heartland 100 tablets — — FDA listed —
Wonderbelly Extra Strength Anti-Gas 125 mg 82431-0201-02 Ginger 2 tablets — — Discontinued —
Wonderbelly Extra Strength Anti-Gas 125 mg 82431-0202-02 Ginger 2 tablets — — Discontinued —
Wonderbelly Extra Strength Anti-Gas 125 mg 82431-0203-02 Ginger 2 tablets — — Discontinued —
Wonderbelly Extra Strength Anti-Gas 82431-0291-10 Ginger 10 tablets — — Discontinued —
Simethicone 125 mg 82804-0152-09 Proficient 9 tablets — — FDA listed —
QCH Extra Strength Gas Relief Cherry Flavor 134CHR 125 mg 83324-0132-18 Chain 9 tablets — — FDA listed —
Gas Relief 125 mg 83324-0325-18 Chain 9 tablets — — FDA listed —
Pepto Gas plus Bloating 125 mg 84126-0378-16 The 16 tablets — — FDA listed —
Maximum Strength Antacid Mint 125 mg 53041-0100-23 Guardian 60 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

🏛️
2016
On the market since
Mar 2016
📍
2026
Currently FDA-listed
10 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.

What it looks like

Color pink / orange / purple
ShapeOval
ImprintMYLG
Size12 mm
ScoringNot scored
FlavorFruit
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.

🧪 Avoiding an ingredient? See Simethicone inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 76A0JE0FKJ
    Adipic acid is an organic compound used in medicines as a buffer and pH regulator. It helps maintain the proper acidity level in the product to keep it stable and improve how the body absorbs the active ingredient.
  • UNII K679OBS311
    Carboxymethylcellulose sodium is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a disintegrant to help the tablet break apart, or a thickener in liquids.
  • UNII 2LRS185U6K
    D&C Red No. 27 is a synthetic red colorant used in medicines and cosmetics. It gives tablets, capsules, or liquids their red or reddish color so products are visually identifiable.
  • 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 H77VEI93A8
    A synthetic yellow dye used to color medications. It helps identify the drug and make it visually distinctive, with no effect on how the medicine works.
  • UNII RFW2ET671P
    Hydroxypropyl cellulose is a plant-derived thickening agent made from cellulose. It acts as a binder to hold tablet ingredients together and as a film-former to coat tablets or control how fast the medicine releases.
  • UNII S870P55O2W
    Isomalt is a sugar alcohol made from sugar that's used as a sweetener and bulking agent in medicines. It helps give tablets and powders the right texture and sweetness while having minimal calories.
  • 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 ETJ7Z6XBU4
    Silicon dioxide is a naturally occurring mineral used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping during manufacturing and storage.
  • 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.
  • UNII C151H8M554
    A natural sugar derived from sugar cane or sugar beets. It's used as a sweetener, filler, and binder to improve taste, add bulk, and help hold tablet or capsule ingredients together.
  • UNII K4C08XP666
    A mineral salt made from calcium and phosphate. It acts as a filler to add bulk and texture to tablets and powders, and also helps stabilize and bind ingredients together.

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

The official label also statesadipic acid, carboxymethylcellulose sodium,D&C red 27 lake, FD&C blue 1 lake, FD &C yellow 6 lake, flavors, hydroxypropyl cellulose, isomalt, magnesium stearate, maltodextrin, silica, sucralose, sucrose, tricalcium phosphate,

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

LabelerInfirst Healthcare Inc.
FDA applicationM002 (OTC MONOGRAPH DRUG)
Labeler code62372
First marketedMar 2016
Product typeHuman Otc Drug
Portfolio17 products on file

More NDCs from Infirst Healthcare Inc. labeler code 62372

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 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses Relieves pressure and bloating commonly referred to as gas

⏱️ Dosage and Administration 33 words ▾

Directions Adults and children 12 years and older : thoroughly chew 3-6 mini-tablets as needed. • do not exceed 12 mini-tablets in 24 hours except under the advice and supervision of a physician.

⚠️ Warnings 14 words ▾

Warnings Keep out of the reach of children. Keep out of reach of children

📦 Storage and Handling 21 words ▾

Other information each dose contains: calcium 75 mg • protect from heat and moisture • store at 20-25° C (68-77° F)

🧪 Active Ingredient 10 words ▾

Active ingredient (in each 3 tablet dose) Simethicone 125 mg

🧪 Inactive Ingredients 32 words ▾

Inactive ingredients adipic acid , carboxymethylcellulose sodium ,D&C red 27 lake, FD&C blue 1 lake, FD &C yellow 6 lake, flavors, hydroxypropyl cellulose, isomalt, magnesium stearate, maltodextrin, silica, sucralose, sucrose, tricalcium phosphate,

🎯 Purpose 2 words ▾

Purpose Anti-gas

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children

📄 Questions or Comments 10 words ▾

Questions or comments? call 1-844-695-6624 toll free (English & Spanish)

📄 Package Label / Principal Display Panel 134 words ▾

Principal Display Panel FREE 20% MORE CONVENIENT POCKET PACK Mylanta ® GAS Minis Fast relief of the bloating , pressure, and discomfort of gas Extra Strength, with the #1 selling medicine for gas relief Great tasting ,chewable mini-tablets in an on-the-go pack Also available in great tasting Arctic Mint & Cherry TAMPER EVIDENT: DO NOT USE MYLANTA GAS MINI-TABLETS IF THE BREAKAWAY BAND ON TOP OF CONTAINER IS BROKEN OR MISSING. Mylanta is a registered trademark of McNeil Consumer Pharmaceuticals Co. Patent pending infirst + HEALTHCARE Manufactured for: Infirst Healthcare Inc.

Westport, CT 06880 © 2016 Infirst Healthcare Inc. Mylanta.com KEEP OUTER PACKAGING FOR COMPLETE LABELING Mylanta GAS Minis 50 tablets Assorted Flavor Package level for 60 chewable tablets MYLGAF60FC MYLANTA GAS RELIEF Mylanta Pouch Pack Label Mylanta Mini Pouch Pack 3 Mini Tablets

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

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 Simethicone — the ingredient across all brands.

Top reported reactions

Chronic Kidney Disease1,159
Nausea723
Diarrhoea673
Fatigue644
Acute Kidney Injury633
Renal Failure583
Pain416

Age at onset

Neonate2
Infant4
Child23
Adolescent17
Adult380
Elderly398

Reporter sex

8,247 reports
Male · 35%
Female · 65%
Unknown · 0%

Serious outcomes

Hospitalization2,709
Life-threatening247
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 402 236
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.

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

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 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 Infirst Healthcare 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 2 other package presentations of this same product, including 3 tablets (62372-0801-03), 50 tablets (62372-0801-50). 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?
Infirst Healthcare 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.
← 62372-0800-50 · Infirst 62379-0005-05 · Simple →
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.