Label: ZEROQ- potassium carbonate liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 80643-0002-1 - Packager: JISANG Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated September 28, 2020
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- 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
ZEROQ
potassium carbonate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80643-0002 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM CARBONATE (UNII: BQN1B9B9HA) (CARBONATE ION - UNII:7UJQ5OPE7D) POTASSIUM CARBONATE 0.5 g in 500 mL Inactive Ingredients Ingredient Name Strength PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80643-0002-1 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 09/21/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/21/2020 Labeler - JISANG Co., Ltd. (694802124) Registrant - JISANG Co., Ltd. (694802124) Establishment Name Address ID/FEI Business Operations JISANG Co., Ltd. 694802124 manufacture(80643-0002)