GAS RELIEF SIMETHICONE 180MG SOFTGEL- simethicone capsule, liquid filled

Gas Relief Simethicone 180mg Softgel by

Drug Labeling and Warnings

Gas Relief Simethicone 180mg Softgel by is a Otc medication manufactured, distributed, or labeled by NUVICARE LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient (in each softgel)

Simethicone 180 mg

Purpose

Antiflatulent (Antigas)

Uses

relieves

• bloating
• pressure
• fullness commonly referred to as gas

Warnings

Stop use and ask a doctor if condition persists.

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

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

• store at 15° to 30°C (59° to 86°F)

Inactive Ingredients

Peppermint oil, Gelatin, Sorbitol, sorbitan anhydrous, Glycerin, Titanium dioxide, FD &C yellow 6/sunset yellow, Black iron oxide.

Questions or Comments?

Call 1 (718) 337-8733 or visit support@nuvicare.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GAS RELIEF SIMETHICONE 180MG SOFTGEL 
simethicone capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84324-015
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
PEPPERMINT OIL (UNII: AV092KU4JH)
GELATIN (UNII: 2G86QN327L)
SORBITOL (UNII: 506T60A25R)
SORBITAN (UNII: 6O92ICV9RU)
GLYCERIN (UNII: PDC6A3C0OX)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
FERROSOFERRIC OXIDE (UNII: XM0M87F357)

Product Characteristics
Color	orange	Score	no score
Shape	OVAL	Size	11mm
Flavor		Imprint Code	910
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84324-015-01	100 in 1 BOTTLE; Type 0: Not a Combination Product	07/18/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M002	07/18/2024

Labeler - NUVICARE LLC (119257565)

Registrant - NUVICARE LLC (119257565)