Ultra Strength Gas Relief

Manufacturer
Meijer Distribution Inc.
Effective date
2024-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:47:47

Label at a glance#

ProductUltra Strength Gas Relief
Active ingredientDIMETHICONE
Label structure6 sections

Indications and uses

for the relief of ■ pressure and bloating commonly referred to as gas

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Uses

INDICATIONS & USAGE SECTION

for the relief of
■ pressure and bloating commonly referred to as gas

Warnings

WARNINGS SECTION

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - QUESTIONS SECTION

Questions or comments? 1-888-333-9792

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active

ingredient in Gas-X®

Ultra Strength Softgels*

Simethicone 180mg

Anti-gas

Fast Relief of:

Bloating

Pressure

Fullness

Gas

Easy to swallow softgels

50 Softgels

CartonCarton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
252294simethicone 180 MG Oral CapsulePSN2
252294simethicone 180 MG Oral CapsuleSCD2
252294dimethicone 180 MG Oral CapsuleSY2

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
79481-0037-5Ultra Strength Gas Relief5 in 1 CARTONCAPSULE, LIQUID FILLED52
79481-0037-5Ultra Strength Gas Relief10 in 1 BLISTER PACKCAPSULE, LIQUID FILLED102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79481-0037ULTRA STRENGTH GAS RELIEF (SIMETHICONE) CAPSULE, LIQUID FILLED [MEIJER DISTRIBUTION INC.]22 package rows20241222_b2475157-216c-48b4-aa3f-be0a8ebdb68d.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
79481-003779481-0037-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
29badb50-4e9d-fdd8-e063-6394a90a099fb2475157-216c-48b4-aa3f-be0a8ebdb68d2024-12-20WarningsExact identifier
spl id: 29badb50-4e9d-fdd8-e063-6394a90a099f
spl set id: b2475157-216c-48b4-aa3f-be0a8ebdb68d

Reported adverse events (FAERS/openFDA)#

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