Label: AFTER BITE KIDS- sodium bicarbonate cream
- NDC Code(s): 90107-1280-1
- Packager: Adventure Ready Brands
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 16, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep Out of Reach of Children.
- Directions
- Inactive Ingredients
- Package Label
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INGREDIENTS AND APPEARANCE
AFTER BITE KIDS
sodium bicarbonate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:90107-1280 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE 1 g in 20 g Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) 1.1 g in 20 g DIMETHICONE (UNII: 92RU3N3Y1O) 0.1 g in 20 g EUCALYPTUS OIL (UNII: 2R04ONI662) 0.26 g in 20 g OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) 0.5 g in 20 g OLETH-10 PHOSPHATE (UNII: Q95361F4VS) 0.28 g in 20 g WATER (UNII: 059QF0KO0R) 14.1 g in 20 g SODIUM HYDROXIDE (UNII: 55X04QC32I) 0.24 g in 20 g TEA TREE OIL (UNII: VIF565UC2G) 0.2 g in 20 g .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.1 g in 20 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:90107-1280-1 1 in 1 BOX 09/01/2020 1 20 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 09/01/2020 Labeler - Adventure Ready Brands (064437304)