Label: SANITALK - SANITIZER(COVID-19)- potassium carbonate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 82486-0001-1, 82486-0001-2 - Packager: Sanitalk Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 14, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SANITALK - SANITIZER(COVID-19)
potassium carbonate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82486-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 0.1 g in 100 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82486-0001-1 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/12/2022 2 NDC:82486-0001-2 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/12/2022 Labeler - Sanitalk Inc (695365740) Registrant - Sanitalk Inc (695365740) Establishment Name Address ID/FEI Business Operations NARO Global Inc. 695123340 manufacture(82486-0001)
