Ultra Strength Gas Relief

Manufacturer
Wal-Mart Stores Inc | Humanwell PuraCap Pharmaceutical (Wuhan) Co., Ltd.
Effective date
2024-11-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:38:37

Label at a glance#

ProductUltra Strength Gas Relief
Active ingredientDIMETHICONE
Label structure9 sections

Dosage and administration

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

Storage and handling

store at controlled room temperature 15º - 30ºC (59º - 86ºF) protect from heat and moisture do not use if imprinted safety seal under cap is broken or missing

Label contents#

Full prescribing information#

Active ingredient (in each softgel)

OTC - ACTIVE INGREDIENT SECTION

Simethicone 180 mg

Purpose

OTC - PURPOSE SECTION

Antigas

Use

INDICATIONS & USAGE SECTION

 for the relief of

  • pressure and bloating commonly referred to as gas

Warnings

WARNINGS SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

STORAGE AND HANDLING SECTION

  • store at controlled room temperature 15º - 30ºC (59º - 86ºF)
  • protect from heat and moisture
  • do not use if imprinted safety seal under cap is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

FD&C yellow#6, gelatin, glycerin, purified water and white ink

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free: 1-888-287-1915

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Ultra Strength Gas Relief

Simethicone 180 mg Anti-gas  50 Softgels

NDC 49035-585-21

*Compare to the active ingredient in Gas-X ®Ultra Strength

WM21-00-frontWM21-00-front

WM21-00-backWM21-00-back

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
49035-585-21Ultra Strength Gas Relief50 in 1 BOTTLECAPSULE, LIQUID FILLED502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-585ULTRA STRENGTH GAS RELIEF (SIMETHICONE) CAPSULE, LIQUID FILLED [WAL-MART STORES INC]2Current NDC, Legacy NDC, 1 package rows20241123_206d57ec-c854-496e-af53-7d8b2a208d85.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49035-585-21EA - Each49035-58575246f54-2a90-460b-a72e-5369e54c5cf112024-02-14

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-58549035-585-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
Ultra Strength Gas ReliefSIMETHICONEWal-Mart Stores Inc206d57ec-c854-496e-af53-7d8b2a208d852024-11-21WarningsExact identifier
ndc (package): 49035-585-21
ndc (product): 49035-585
ndc11 (package): 49035058521
spl id: 2778861c-cfab-4b77-e063-6394a90ad42c
spl set id: 206d57ec-c854-496e-af53-7d8b2a208d85

Reported adverse events (FAERS/openFDA)#

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