Label: SIMETHICONE GAS RELIEF- simethicone suspension/ drops
- NDC Code(s): 71444-788-01
- Packager: MOM Enterprises, LCC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 9, 2024
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INGREDIENTS AND APPEARANCE
SIMETHICONE GAS RELIEF
simethicone suspension/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71444-788 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 GINGER (UNII: C5529G5JPQ) STEVIA LEAF (UNII: 6TC6NN0876) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) POLYSORBATE 60 (UNII: CAL22UVI4M) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) XANTHAN GUM (UNII: TTV12P4NEE) SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X) WATER (UNII: 059QF0KO0R) Product Characteristics Color white (homogenous white viscous liquid) Score Shape Size Flavor GINGER (sweet) Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71444-788-01 1 in 1 CARTON 08/01/2017 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 M002 08/01/2017 Labeler - MOM Enterprises, LCC (135903776)
