Label: FACE-BODY-S- potassium carbonate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 71957-0003-1 - Packager: NARO, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated January 1, 2018
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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
FACE-BODY-S
potassium carbonate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71957-0003 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 WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71957-0003-1 80 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/02/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 01/02/2018 Labeler - NARO, INC. (694590211) Registrant - NARO, INC. (694590211) Establishment Name Address ID/FEI Business Operations NARO, INC. 694590211 manufacture(71957-0003)
