Label: AFTER BITE ADVANCED- sodium bicarbonate liquid
- NDC Code(s): 90107-1103-1
- Packager: Adventure Ready Brands
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 19, 2023
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- Drug Facts
- Active Ingredient
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- Inactive Ingredients
- After Bite
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INGREDIENTS AND APPEARANCE
AFTER BITE ADVANCED
sodium bicarbonate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:90107-1103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM BICARBONATE (UNII: 8MDF5V39QO) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM BICARBONATE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength AMMONIA (UNII: 5138Q19F1X) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:90107-1103-1 1 in 1 BOX 01/01/2021 1 14 mL 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 final part347 01/01/2021 Labeler - Adventure Ready Brands (064437304) Registrant - Adventure Ready Brands (064437304) Establishment Name Address ID/FEI Business Operations Adventure Ready Brands 064437304 manufacture(90107-1103)