Wonderbelly Extra Strength Anti-Gas Simethicone 125 mg Tablet, Chewable, 10-count
by Ginger Health Company · 10 TABLET, CHEWABLE in 1 BOTTLE (82431-202-10)
NDC 82431-0202-10
🏷️ FDA NDC (as labeled)
82431-202-10
billing pads the product segment with a zero
This package
Contains10-count
Pack sizes4 compare ↓
OTC
Discontinued
Non-controlled
⚠ Inactivated by FDA
🗂️ 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 →
⚠️
Excluded from the active FDA NDC Directory.
FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
82431-202-10
Product NDC
82431-202
11-digit billing NDC
82431020210
RxCUI
314221
UNII
92RU3N3Y1O
Application #
M002
SPL Set ID
0c568358-3716-7c68-e063-6394a90a30d0
Physiologic effect
Skin Barrier Activity
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Inactivated by FDA (certified through Dec 2026)
Marketing start
2024-03-01
Route
ORAL
Dosage form
TABLET, CHEWABLE
Substance
DIMETHICONE
Why two NDCs?
The FDA registers this code as 82431-202-10 — 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 → 82431-0202-10. 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
LabelerGinger Health Company
FDA applicationM002 (OTC MONOGRAPH DRUG)
Labeler code82431
First marketedMar 2024
Product typeHuman Otc Drug
Portfolio17 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
📗 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?
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Simethicone — tap one for details:
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.
💬 Questions about Simethicone?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 What it looks like
Color
white
ShapeRectangle
ImprintW;202
Size17 mm
ScoringNot scored
FlavorMango
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.
💲 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 system | Per each | Per 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price 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 | $0.104 | — | Availability likely | — |
| extra strength Gas Relief cherry creme 125 mg 46122-0811-08 | Amerisource | 9 tablets | $0.104 | — | Availability likely | — |
| Foster and Thrive Extra Strength Gas Relief Cherry 125 mg 70677-1077-01 | Strategic | 9 tablets | $0.104 | — | 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-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 mgthis 82431-0202-10 | Ginger | 10 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
🏛️
2024
On the market since
Mar 2024
📍
2026
Currently FDA-listed
2 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.
🔬 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
Reporter sex
Male · 35%
Female · 65%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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 NDC | Description | Marketing start | Status |
|---|---|---|---|
| 82431-0202-02 | 2 TABLET, CHEWABLE in 1 POUCH (82431-202-02) | 2024-09-01 | Inactivated by FDA |
| 82431-0202-10 You're viewing this | 10 TABLET, CHEWABLE in 1 BOTTLE (82431-202-10) | 2025-02-01 | Inactivated by FDA |
| 82431-0202-35 | 1 BOTTLE in 1 CARTON (82431-202-35) / 35 TABLET, CHEWABLE in 1 BOTTLE | 2025-03-01 | Inactivated by FDA |
| 82431-0202-42 | 42 TABLET, CHEWABLE in 1 BOTTLE (82431-202-42) | 2025-03-01 | Inactivated by FDA |
Pack size FAQ
What quantity is in NDC 82431-0202-10?
NDC 82431-0202-10 is a 10-count package — 10 tablet, chewable in 1 bottle.
What is the difference between NDC 82431-0202-10 and NDC 82431-0202-02?
Both are Wonderbelly Extra Strength Anti-Gas Simethicone 125 mg Tablet, Chewable — the drug itself is identical. NDC 82431-0202-10 is the 10-count package, while NDC 82431-0202-02 is the 2 tablets package.
What NDC number is used to bill for this package of Wonderbelly Extra Strength Anti-Gas Simethicone 125 mg Tablet, Chewable?
Bill NDC 82431-0202-10 — the 11-digit billing format is 82431020210. 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
No longer marketed (per FDA listing data)
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
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 82431-202-10, 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: 82431-0202-10, written without dashes as 82431020210. 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 82431-0202-10, the first segment (82431) is the labeler code FDA assigned to Ginger Health Company; the middle segment (0202) 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.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 2 tablets (82431-0202-02), 35 tablets (82431-0202-35), 42 tablets (82431-0202-42). 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?
Ginger Health Company 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
🧪 Active Ingredient
🧪 Inactive Ingredients
🎯 Purpose
🎯 Indications and Usage ▾
Uses relieves pressure bloating fullness commonl referred to as gas
⏱️ Dosage and Administration ▾
Directions chew or crush tablets completely before swallowing. Do not swallow tablets whole. adults and children 12 years of age and older: chew 1-2 tablets as symptoms occur, or as directed by a doctor do not take more than 4 tablets in a 24-hour period except under the advice and supervision of a doctor
⚠️ Warnings ▾
Warnings If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children.
🧪 Active Ingredient ▾
Active Ingredient (in each tablet) Simethicone 125 mg
🧪 Inactive Ingredients ▾
Inactive ingredients calcium carbonate, calcium phosphate, corn starch, natural flavors, sucrose, vegetable magnesium stearate
🎯 Purpose ▾
Purpose Anti-gas
No label section mentions that — try another word, or open the full label on DailyMed below.
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.