Label: AMMONIASPORT RAW- ammonia 2% liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 73395-197-01 - Packager: AmmoniaSport LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 18, 2020
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- Official Label (Printer Friendly)
- WARNINGS AND PRECAUTIONS
- Active Ingredient
- Purpose
- Use
- Warnings
- If pregnant or nursing a baby
- Keep out of the reach of children
- Directions
- Inactive Ingredients
- Other Information
- Questions or Comments?
- Label
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INGREDIENTS AND APPEARANCE
AMMONIASPORT RAW
ammonia 2% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73395-197 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIA (UNII: 5138Q19F1X) (AMMONIA - UNII:5138Q19F1X) AMMONIA 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ) SODIUM CARBONATE (UNII: 45P3261C7T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73395-197-01 31 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/01/2020 Labeler - AmmoniaSport LLC (048476710) Registrant - AmmoniaSport LLC (048476710) Establishment Name Address ID/FEI Business Operations James Alexander Corp 040756421 manufacture(73395-197)