Quality Choice Infants Non-Staining Gas Relief 

Quality Choice Infants Non-staining Gas relief by

Drug Labeling and Warnings

Quality Choice Infants Non-staining Gas relief by is a Otc medication manufactured, distributed, or labeled by Chain Drug Marketing Association Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

QUALITY CHOICE INFANTS NON-STAINING GAS RELIEF- simethicone solution/ drops 
Chain Drug Marketing Association Inc.

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Quality Choice Infants Non-Staining Gas Relief 

ACTIVE INGREDIENT (in each 0.3 mL)

Simethicone 20 mg

PURPOSE

Antigas

USE(S)

relieves the symptoms of gas frequently caused by air swallowing or certain formulas or foods

WARNINGS

When using this product do not exceed 12 doses per day

KEEP OUT OF REACH OF CHILDREN

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

DIRECTIONS

• shake well before using
• all dosages may be repeated as needed, after meals and at bedtime 
• fill enclosed dropper to recommended dosage level
• dispense liquid slowly into baby's mouth, toward the inner cheek
• may mix with 1 oz. of cool water, infant formula or other suitable liquids
• clean dropper after each use and close the bottle to maintain child resistance

age (yr)	weight (lb)	dose
infants under 2	under 24	0.3 mL
children over 2	over 24	0.6 mL

OTHER INFORMATION

store at room temperature

INACTIVE INGREDIENTS

benzoic acid, flavor, magnesium aluminum silicate, purified water, simethicone emulsion, sorbitol, xanthan gum

PRINCIPAL DISPLAY PANEL

NDC: 63868-112-01

QC

Quality Choice 

*Compare to the Active Ingredient in Mylicon®

Non-Staining Infants' Drops

Infants' Non-Staining

Gas Relief Drops

Antigas

Simethicone 20 mg

Fast Relief of Gas Symptoms 

No Artificial Flavor 

Alcohol Free

Dye Free

Gentle & Safe**

**Use only as directed;

do not exceed 12 doses per day.

1 FL OZ (30mL)

QUALITY CHOICE INFANTS NON-STAINING GAS RELIEF 
simethicone solution/ drops

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-112
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	20 mg  in 0.3 mL

Inactive Ingredients
Ingredient Name	Strength
BENZOIC ACID (UNII: 8SKN0B0MIM)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	WHITE (off-white)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-112-01	1 in 1 CARTON	07/29/2022	12/18/2024
1		30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M001	07/29/2022	12/18/2024

Labeler - Chain Drug Marketing Association Inc. (011920774)

Establishment
Name	Address	ID/FEI	Business Operations
Guardian Drug Company		119210276	manufacture(63868-112)

Revised: 12/2024

Document Id: 18e5ebbe-0915-43ae-9b08-c5fed98d150e

34390-5

Set id: f956aff6-1d65-4639-81c7-3116c37b777a

Version: 2

Effective Time: 20241218