Label: 100% PURE HAND SANITIZER HYDRATING- ethyl alcohol gel
- NDC Code(s): 52667-011-01, 52667-011-02
- Packager: Purity Cosmetics
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 19, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
- Warnings:
- STORAGE AND HANDLING
- WHEN USING
- KEEP OUT OF REACH OF CHILDREN
- OTHER SAFETY INFORMATION
- STOP USE
- Directions:
- Other Ingredients:
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
100% PURE HAND SANITIZER HYDRATING
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52667-011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) GUARAPROLOSE (1300 MPA.S AT 1%) (UNII: 1530WMS90S) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52667-011-01 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/03/2020 02/09/2025 2 NDC:52667-011-02 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/03/2020 02/09/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug 505G(a)(3) 08/03/2020 02/09/2025 Labeler - Purity Cosmetics (055795259) Registrant - Our Babylon LLC (105266218) Establishment Name Address ID/FEI Business Operations Our Babylon LLC 105266218 manufacture(52667-011)