GNP REGULAR STRENGTH GAS RELIEF- dimethicone tablet, chewable

GNP Regular Strength Gas Relief by

Drug Labeling and Warnings

GNP Regular Strength Gas Relief by is a Otc medication manufactured, distributed, or labeled by ATLANTIC BIOLOGICALS CORP., UNIT DOSE SOLUTIONS. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient (in each tablet)

Simethicone 80 mg

Purpose

Antigas

HOW SUPPLIED

NDC: 17856-1118-1

regular strength

Gas Relief

Anti-gas

fast relief of: pressure, bloating & gas distress

mint

50 chewable tablets (80 mg ea.)

KEEP OUT OF REACH OF CHILDREN

Uses

relieves:

• pressure
• bloating
• symptoms referred to as gas

Warnings

Keep out of reach of children.In case of overdose, get medical help or contact a poison control center immediately.

Directions

• chew 2 to 4 tablets thoroughly as needed after meals and at bedtime.
• do not exceed 6 tablets per day unless directed by a physician.

Other information

• do not use if inner seal is broken.
• store at room temperature
• avoid high humidity and excessive heat, above 40 0C (104 0F)

Inactive ingredients

compressible sugar, dextrose, flavor, magnesium stearate, maltodextrin, microcrystalline cellulose, sorbitol

DISTRIBUTED BY: 

ATLANTIC BIOLOGICALS CORP.

MIAMI, FL 33179

PDP

INGREDIENTS AND APPEARANCE

GNP REGULAR STRENGTH GAS RELIEF 
dimethicone tablet, chewable

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 17856-1118(NDC:24385-118)
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
RAW SUGAR (UNII: 8M707QY5GH)
DEXTROSE (UNII: IY9XDZ35W2)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SORBITOL (UNII: 506T60A25R)

Product Characteristics
Color	white	Score	no score
Shape	CAPSULE (round tablet)	Size	13mm
Flavor	MINT	Imprint Code	G103
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 17856-1118-1	50 in 1 BOX	04/21/2022
1	NDC: 17856-1118-2	1 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M002	08/08/2011

Labeler - ATLANTIC BIOLOGICALS CORP. (047437707)

Registrant - ATLANTIC BIOLOGICALS CORP. (047437707)

Establishment
Name	Address	ID/FEI	Business Operations
UNIT DOSE SOLUTIONS		360804194	repack(17856-1118)