GAS RELIEF ULTRA STRENGTH- simethicone capsule, liquid filled 
Walgreens

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Drug Facts

Active ingredient (in each softgel)

Simethicone 180 mg

Purpose

Antigas

Uses

For the relief of 

Warnings

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

Directions

Other information

Inactive ingredients

FD&C red #40*, FD&C yellow #6, gelatin, glycerin

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal display panel

Compare to the active ingredient in Gas-X® Ultra Strengt Softgels††

Gas Relief

SIMETHICONE 180 mg ANTIGAS

Ultra Strength

SOFTGELS

††This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Gas-X® Ultra Strength Softgels.

TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.

DISTRIBUTED BY:WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

Package Label

Simethicone 180 mg

WALGREENS Ultra Strength Gas Relief

GAS RELIEF  ULTRA STRENGTH
simethicone capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-8740
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE180 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
GELATIN (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
Product Characteristics
ColororangeScoreno score
ShapeOVALSize12mm
FlavorImprint Code 05A
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-8740-5050 in 1 CARTON05/29/2020
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:0363-8740-2020 in 1 CARTON05/29/2020
21 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00205/29/2020
Labeler - Walgreens (008965063)

Revised: 6/2024
Document Id: feea11bf-15fa-447a-820e-280f9cea9151
Set id: 0050b639-5fb6-4503-ae73-e319cf037027
Version: 5
Effective Time: 20240626
 
Walgreens