Label: ALLPEAU PURE HAND SANITIZER- alcohol hand sanitizer gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75567-1011-1 - Packager: WID Cosmetics (Shanghai) Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 27, 2020
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- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
ALLPEAU PURE HAND SANITIZER
alcohol hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75567-1011 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 42 mL in 60 mL Inactive Ingredients Ingredient Name Strength HOUTTUYNIA CORDATA FLOWERING TOP (UNII: RH041UUZ22) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) CUCUMBER (UNII: YY7C30VXJT) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) ALOE VERA LEAF (UNII: ZY81Z83H0X) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75567-1011-1 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/27/2020 Labeler - WID Cosmetics (Shanghai) Co., Ltd. (554443373) Registrant - A03 Lab of BTS (548009541) Establishment Name Address ID/FEI Business Operations WID Cosmetics (Shanghai) Co., Ltd. 554443373 manufacture(75567-1011) , label(75567-1011)