Label: HAND SANITIZER GEL(AG)- hand sanitizer gel
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Contains inactivated NDC Code(s)
NDC Code(s): 54039-001-01 - Packager: Anhui Wanxing Industry Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated May 12, 2020
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- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
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- PURPOSE
- WARNINGS
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INGREDIENTS AND APPEARANCE
HAND SANITIZER GEL(AG)
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:54039-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SILVER CATION (UNII: 57N7B0K90A) (SILVER CATION - UNII:57N7B0K90A) SILVER CATION 10 g in 500 mL Inactive Ingredients Ingredient Name Strength GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) METHYL BENZOATE (UNII: 6618K1VJ9T) Product Characteristics Color Score Shape Size Flavor Imprint Code SILVERELF Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:54039-001-01 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/11/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 05/11/2020 Labeler - Anhui Wanxing Industry Co.,Ltd. (540397995) Establishment Name Address ID/FEI Business Operations Anhui Wanxing Industry Co.,Ltd. 540397995 manufacture(54039-001)