Label: HAND SANITIZER- ethyl alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73357-627-00, 73357-627-01, 73357-627-02, 73357-627-03, view more73357-627-05, 73357-627-08, 73357-627-09, 73357-627-10, 73357-627-15, 73357-627-20, 73357-627-24, 73357-627-25, 73357-627-29, 73357-627-30, 73357-627-35, 73357-627-50, 73357-627-51, 73357-627-55, 73357-627-60, 73357-627-80 - Packager: Hangzhou Lanqueen Cosmetics 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 10, 2020
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- Drug Facts
- Active Ingredients:
- PURPOSE
- Uses:
- Warning:
- Directions:
- Inactive Ingredients:
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
ethyl alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73357-627 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) TROLAMINE (UNII: 9O3K93S3TK) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73357-627-10 10 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 2 NDC:73357-627-15 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 3 NDC:73357-627-30 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 4 NDC:73357-627-60 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 5 NDC:73357-627-80 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 6 NDC:73357-627-00 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 7 NDC:73357-627-08 8 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 8 NDC:73357-627-29 29 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 9 NDC:73357-627-20 120 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 10 NDC:73357-627-50 150 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/15/2019 11 NDC:73357-627-05 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 12 NDC:73357-627-02 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 13 NDC:73357-627-24 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 14 NDC:73357-627-25 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 15 NDC:73357-627-03 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 16 NDC:73357-627-35 350 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 17 NDC:73357-627-51 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 18 NDC:73357-627-01 20 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 19 NDC:73357-627-55 5 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 20 NDC:73357-627-09 90 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/17/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/15/2019 Labeler - Hangzhou Lanqueen Cosmetics Co., Ltd. (542984409) Establishment Name Address ID/FEI Business Operations Hangzhou Lanqueen Cosmetics Co., Ltd. 542984409 manufacture(73357-627)