Label: DR. DRIS HAND SANITIZER- ethyl alcohol liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 81383-001-01, 81383-001-02, 81383-001-03, 81383-001-04 - Packager: Hanson Venture Enterprise Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 13, 2021
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Purpose
- Uses
- Warnings
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- Inactive Ingredients
- Questions or Comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DR. DRIS HAND SANITIZER
ethyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81383-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 2720 mL in 4000 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE VERA LEAF (UNII: ZY81Z83H0X) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) PEPPERMINT OIL (UNII: AV092KU4JH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81383-001-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/13/2021 2 NDC:81383-001-02 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/13/2021 3 NDC:81383-001-03 475 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/13/2021 4 NDC:81383-001-04 4000 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/13/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 01/13/2021 Labeler - Hanson Venture Enterprise Inc. (204263995) Establishment Name Address ID/FEI Business Operations Natures Formulae Health Products Ltd. 241385587 manufacture(81383-001)