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Firstcare Gas Relief Simethicone 125 mg Anti-gas 125 mg Tablet, Chewable, 100-count — NDC 71594-0709-10 package photo

Firstcare Gas Relief Simethicone 125 mg Anti-gas 125 mg Tablet, Chewable, 100-count

by USpharma Ltd · 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71594-709-10)
NDC 71594-0709-10
🏷️ FDA NDC (as labeled) 71594-709-10 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 71594-709-10
Product NDC 71594-709
11-digit billing NDC 71594070910
RxCUI 314221
UNII 92RU3N3Y1O
Application # M002
SPL Set ID e92c9661-01f2-42be-af54-42e60efcae35
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 2026-05-12
Route ORAL
Dosage form TABLET, CHEWABLE
Substance DIMETHICONE
Why two NDCs? The FDA registers this code as 71594-709-10 — 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 → 71594-0709-10. 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.

🏭 Manufacturer & labeler

LabelerUSpharma Ltd
FDA applicationM002 (OTC MONOGRAPH DRUG)
Labeler code71594
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio3 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

📖 What it is MedlinePlus · NLM

Simethicone is used to treat the symptoms of gas such as uncomfortable or painful pressure, fullness, and bloating. 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
  • Simethicone works to relieve the uncomfortable pressure, bloating, and full or stuffed feeling that comes from trapped gas in your stomach or intestines. It's used when gas builds...
  • What exactly does simethicone do for gas?
  • Yes — there are infant-specific simethicone products, like Mylicon Infants Gas Relief and similar infant drops, designed just for babies. They're used to relieve gas discomfort tha...
  • Can I give simethicone drops to my baby?
📖 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.

💊 What it looks like

Color white
ShapeRound
Imprint5
Size12 mm
ScoringScored — splits in 2
FlavorCherry
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 XF417D3PSL
    Anhydrous citric acid is a sour, crystalline powder derived from citric acid with water removed. In medicines, it acts as a buffer to control pH, adds tartness to improve taste, and helps tablets disintegrate.
  • UNII R12CBM0EIZ
    A natural wax derived from a Brazilian palm tree, used as a coating and polish on tablets and capsules. It creates a smooth, shiny finish that protects the medicine and improves appearance.
  • UNII 9G5L16BK6N
    A thick, sweet liquid made from corn starch. It acts as a sweetener, thickener, and binder in medicines, helping create the right texture and taste while holding ingredients together.
  • UNII M28OL1HH48
    Croscarmellose sodium is a plant-based substance derived from cellulose. It acts as a disintegrant, helping tablets and capsules break down quickly in the digestive system so the medicine can be absorbed.
  • 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 PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII D65DG142WK
    Maltitol is a sugar alcohol made by hydrogenating maltose. It's used as a sweetener and filler in medicines to improve taste and add bulk to tablets and capsules.
  • UNII 3OWL53L36A
    A natural sugar alcohol derived from seaweed or synthesized in the lab. It's used as a filler to add bulk, a sweetener in sugar-free formulas, and a disintegrant to help tablets break apart in the stomach.
  • 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 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.
  • UNII 91D9GV0Z28
    A mineral salt made from calcium and phosphate. It acts as a filler to add bulk to the tablet or capsule, and helps bind ingredients together so the medicine holds its shape.

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

The official label also statesanhydrous citric acid, carnauba wax, corn syrup solids, croscarmellose sodium, crospovidone, glycerin, maltitol syrup, mannitol, microcrystalline cellulose, starch, sucralose, trisodium calcium 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.

💲 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.
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
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 mg 62372-0801-03 Infirst 3 tablets — — Discontinued —
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-gasthis 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 —
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

🏛️
2026
On the market since
May 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Firstcare Gas Relief Simethicone 125 mg Anti-gas (this brand).

Top reported reactions

Blindness1
Conjunctivitis1
Gastritis Erosive1
Haemolytic Anaemia1
Hospice Care1
Inflammation1
Pulmonary Embolism1

Reporter sex

6 reports
Male · 80%
Female · 20%
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2 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
71594-0709-10 You're viewing this 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (71594-709-10) 2026-05-12 Active

🧭 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 FDA registers it as 71594-709-10, 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: 71594-0709-10, written without dashes as 71594070910. 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 71594-0709-10, the first segment (71594) is the labeler code FDA assigned to USpharma Ltd; the middle segment (0709) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (10) 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 USpharma Ltd. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
USpharma Ltd 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 14 words ▾

Uses for the relief of pressure, bloating, and fullness commonly referred to as gas

⏱️ Dosage and Administration 37 words ▾

Directions adults and children 12 years and older: take 1 or 2 chewables as needed after meals and at bedtime. do not exceed 4 chewables in 24 hours except under the advice and supervision of a physician.

⚠️ Warnings 22 words ▾

Warnings Keep out of reach of children. In case of accidental overdose, seek professional assistance or contact a poison control center immediately.

🧪 Active Ingredient 8 words ▾

Active ingredient (in each chewable) Simethicone, 125 mg

🧪 Inactive Ingredients 24 words ▾

Inactive ingredients: anhydrous citric acid, carnauba wax, corn syrup solids, croscarmellose sodium, crospovidone, glycerin, maltitol syrup, mannitol, microcrystalline cellulose, starch, sucralose, trisodium calcium phosphate.

🎯 Purpose 2 words ▾

Purpose Antigas

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.