Label: PURPLE TEETH POWDER powder
- NDC Code(s): 84025-039-01
- Packager: Guangzhou Yanxi Biotechnology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 3, 2024
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- DOSAGE & ADMINISTRATION
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- PURPOSE
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
PURPLE TEETH POWDER
purple teeth powder powderProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84025-039 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDRATED SILICA (UNII: Y6O7T4G8P9) (HYDRATED SILICA - UNII:Y6O7T4G8P9) HYDRATED SILICA 5 mg in 100 g ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 3 mg in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Product Characteristics Color Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:84025-039-01 100 g in 1 BOTTLE; Type 0: Not a Combination Product 06/03/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 06/03/2024 Labeler - Guangzhou Yanxi Biotechnology Co., Ltd (632583102) Establishment Name Address ID/FEI Business Operations Guangzhou Yanxi Biotechnology Co., Ltd 632583102 manufacture(84025-039)