GAS RELIEF- simethicone tablet, chewable

GAS RELIEF by

Drug Labeling and Warnings

GAS RELIEF by is a Otc medication manufactured, distributed, or labeled by Proficient Rx LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Simethicone 80 mg

Purpose

Anti-Gas

Uses

for the relief of

• pressure, bloating, and fullness commonly referred to as gas

Warnings

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

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions

chew thoroughly
adults and children 12 years and over: take 1-2
tablets as needed after meals and at bedtime. Do
not exceed 6 tablets in 24 hours except under the
advice and supervision of a doctor.
children under 12 years: ask a doctor

Other information

• Tamper Evident: Do not use if imprinted seal under cap is missing or broken
• store at room temperature, 15°C - 30°C (59˚F - 86˚F)

Inactive ingredients

dextrose, sugar, maltodextrin, microcrystalline cellulose, peppermint flavor, silica, sorbitol, stearic acid

Questions or comments?

1-800-540-3765

package Label

INGREDIENTS AND APPEARANCE

GAS RELIEF 
simethicone tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71205-737(NDC:57896-799)
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	80 mg

Inactive Ingredients
Ingredient Name	Strength
DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SORBITOL (UNII: 506T60A25R)
STEARIC ACID (UNII: 4ELV7Z65AP)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	13mm
Flavor	PEPPERMINT	Imprint Code	AP019
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71205-737-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	12/28/2022
2	NDC: 71205-737-60	60 in 1 BOTTLE; Type 0: Not a Combination Product	12/28/2022
3	NDC: 71205-737-90	90 in 1 BOTTLE; Type 0: Not a Combination Product	12/28/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M002	02/01/2020

Labeler - Proficient Rx LP (079196022)

Establishment
Name	Address	ID/FEI	Business Operations
Proficient Rx LP		079196022	REPACK(71205-737) , RELABEL(71205-737)