GOOD SENSE GAS RELIEF- simethicone capsule, liquid filled

Drug Labeling and Warnings

Drug Details [pdf]

Active ingredient (in each softgel)

Simethicone 180 mg

Purpose

Anti-gas

Use

• relieves bloating, pressure or fullness commonly referred to as gas

Warnings

Stop use and ask a doctor if

condition persists

Keep out of reach of children.

Directions

• swallow one or two softgels as needed after a meal
• do not exceed two softgels per day except under the advice and supervision of a physician

Other information

• each softgel contains: potassium 5 mg
• store at 68°-77°F (20°-25°C)

Inactive ingredients

FD&C red no. 40, FD&C yellow no. 6, gelatin, glycerin

Questions or comments?

1-800-719-9260

Principal Display Panel

GOODSENSE®

Ultra Strength

Gas Relief

Anti-Gas

Simethicone 180 mg

Actual Size

Relieves Gas Fast

● Pressure

● Bloating

● Discomfort

Easy to Swallow

Compare to active ingredient of Ultra Strength Phazyme®

60 Softgels (180 mg)

Repackaged By: Preferred Pharmaceuticals Inc.

68788-4101

INGREDIENTS AND APPEARANCE

GOOD SENSE GAS RELIEF 
simethicone capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68788-4101(NDC:0113-0657)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE, UNSPECIFIED	180 mg

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
GLYCERIN (UNII: PDC6A3C0OX)

Product Characteristics
Color	ORANGE	Score	no score
Shape	OVAL	Size	9mm
Flavor		Imprint Code	L657
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68788-4101-3	30 in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2026
2	NDC: 68788-4101-6	36 in 1 BOTTLE; Type 0: Not a Combination Product	04/20/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M002	04/20/2026

Labeler - Preferred Pharmaceuticals Inc. (791119022)

Registrant - Preferred Pharmaceuticals Inc. (791119022)

Establishment
Name	Address	ID/FEI	Business Operations
Preferred Pharmaceuticals Inc.		791119022	REPACK(68788-4101)