extra strength gas relief simethicone 125 mg

Manufacturer
Target Corporation
Effective date
2024-12-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:50:10

Label at a glance#

Productextra strength gas relief simethicone 125 mg
Active ingredientDIMETHICONE
Label structure8 sections

Dosage and administration

adults: swallow with water 1 or 2 softgels as needed after meals and at bedtime. do not exceed 4 softgels in 24 hours except under the advice and supervision of a physician.

Storage and handling

store at controlled room temperature 20°-25°C (68°-77°F) protect from light, heat, and moisture

Label contents#

Full prescribing information#

Active ingredient (in each softgel)

OTC - ACTIVE INGREDIENT SECTION

Simethicone 125 mg

Purpose

OTC - PURPOSE SECTION

Antigas

Use

INDICATIONS & USAGE SECTION

for the relief of

  • pressure, bloating, and fullness commonly referred to as gas

Directions

DOSAGE & ADMINISTRATION SECTION

adults:

  • swallow with water 1 or 2 softgels as needed after meals and at bedtime.
  • do not exceed 4 softgels in 24 hours except under the advice and supervision of a physician.

Other information

STORAGE AND HANDLING SECTION

  • store at controlled room temperature 20°-25°C (68°-77°F)
  • protect from light, heat, and moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C blue#1, FD&C yellow#10, gelatin, glycerin, peppermint oil, povidone,
purified water, sorbitol sorbitan, titanium dioxide

Questions or comments?

OTC - QUESTIONS SECTION

1-888-333-9792

Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

This product is not manufactured or distributed by GlaxoSmithKline, owner of the
registered trademark Extra Strength Gas-X®.

Distributed by Target Corporation
Minneapolis, MN 55403
Made in India
TM & ©2022 Target Brands, Inc.

TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER
UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING
KEEP OUTER CARTON FOR COMPLETE WARNINGS
AND PRODUCT INFORMATION

Carton

CartonCarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
198852simethicone 125 MG Oral CapsulePSN5
198852simethicone 125 MG Oral CapsuleSCD5
198852dimethicone 125 MG Oral CapsuleSY5

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DIMETHICONE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11673-415-72extra strength gas relief simethicone 125 mg3 in 1 CARTONCAPSULE, LIQUID FILLED35
11673-415-72extra strength gas relief simethicone 125 mg24 in 1 BLISTER PACKCAPSULE, LIQUID FILLED245

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-415EXTRA STRENGTH GAS RELIEF SIMETHICONE 125 MG CAPSULE, LIQUID FILLED [TARGET CORPORATION]5Legacy NDC, 2 package rows20250101_d117c8d6-f91b-59d5-e053-2995a90acae1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11673-41511673-415-72

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2a817539-2c51-26b4-e063-6294a90abcaad117c8d6-f91b-59d5-e053-2995a90acae12024-12-30WarningsExact identifier
spl id: 2a817539-2c51-26b4-e063-6294a90abcaa
spl set id: d117c8d6-f91b-59d5-e053-2995a90acae1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.