Label: WALGREENS INFANTS DYE FREE GAS RELIEF- simethicone emulsion
- NDC Code(s): 0363-0790-30
- Packager: WALGREEN CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- Active ingredient (in each 0.3 mL)
- Purpose
- Uses
- Warnings
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Directions
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- shake well before using
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- find right dose on chart below. if possible, use weight to dose; otherwise use age.
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- only use the enclosed syringe. Do not use other syringe, dropper, spoon or dosing device when giving this medicine to your child.
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- remove cap and insert syringe into the bottle.
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- pull syringe up until filled to the prescribed level, if you pass the prescribed level, simply push syringe back until you have reached the desired level, Slowly dispense the liquid into your child’s mouth (towards inner cheek)
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- all dosages may be repeated needed, after meals and at bedtime or as directed by a physician.
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- do not exceed 12 doses per day.
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- dosage can also be mixed with 1 oz. cool water, infant formula or other suitable liquids
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- replace cap tightly to maintain child resistance
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- mL= milliliter
Age (yr)
Weight (lb)
Dose( mL)
infants under 2
under 24
0.3
children over 2
over 24
0.6
- Other information
- Inactive ingredients
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Principal Display Panel
Walgreens
Compare to infant’s Mylicon Gas Relief active ingredient††
Infants'
Dye- Free
Gas Relief
Simethicone 20 mg PER DOSE /ANTI-GAS
- DYE FREE
- NONSTAINING FORMULA
- ALCOHOL FREE
- •
- No saccharin
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- No artificial flavor
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- Includes dosing syringe
100 DOSES DYE FREE
1 FL OZ (30 mL)
200 WILMOT RD., DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
Walgreens.com ©2017 Walgreen Co,
WALGREENS PHARMACIST RECOMMENDED‡
‡Walgreens Pharmacist Survey
‡‡ This product is not manufactured or distributed by infirst Healthcare Inc., the distributor of Infants’ Mylicon® Gas Relief.
- IMPORTANT: KEEP THIS CARTON FOR FUTURE REFERENCE ON FULL LABELING
-
INGREDIENTS AND APPEARANCE
WALGREENS INFANTS DYE FREE GAS RELIEF
simethicone emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0790 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE, UNSPECIFIED 20 mg in 0.3 mL Inactive Ingredients Ingredient Name Strength CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 60 (UNII: CAL22UVI4M) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) SORBITOL (UNII: 506T60A25R) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color WHITE (white to off white, opaque) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0790-30 1 in 1 CARTON 08/30/2017 1 30 mL in 1 BOTTLE; 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 08/30/2017 Labeler - WALGREEN CO. (008965063)
