Label: HAND SANITIZER ORIGINAL- alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 76114-004-01 - Packager: Zhejiang Aidi Cosmetics Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated April 24, 2020
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- SPL UNCLASSIFIED SECTION
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER ORIGINAL
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:76114-004 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 GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) CARBOMER 934 (UNII: Z135WT9208) TRIETHANOLAMINE SULFATE (UNII: MV1V89M17O) ALOE VERA WHOLE (UNII: KIZ4X2EHYX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:76114-004-01 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/23/2020 Labeler - Zhejiang Aidi Cosmetics Co., Ltd (530876820) Registrant - Zhejiang Aidi Cosmetics Co., Ltd (530876820) Establishment Name Address ID/FEI Business Operations Zhejiang Aidi Cosmetics Co., Ltd 530876820 manufacture(76114-004)