Label: HAND SANITIZER spray
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Contains inactivated NDC Code(s)
NDC Code(s): 74159-004-01, 74159-004-02, 74159-004-03, 74159-004-04, view more74159-004-05, 74159-004-06, 74159-004-07, 74159-004-08, 74159-004-09 - Packager: Guangzhou BEAVER Cosmetic 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 May 26, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- Do not use
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
hand sanitizer sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74159-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 80 mL in 100 mL Inactive Ingredients Ingredient Name Strength HYDROGEN PEROXIDE (UNII: BBX060AN9V) WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74159-004-01 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 2 NDC:74159-004-02 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 3 NDC:74159-004-03 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 4 NDC:74159-004-04 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 5 NDC:74159-004-05 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 6 NDC:74159-004-06 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 7 NDC:74159-004-07 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 8 NDC:74159-004-08 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 9 NDC:74159-004-09 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/26/2020 Labeler - Guangzhou BEAVER Cosmetic Co.,Ltd. (420020595) Registrant - Guangzhou BEAVER Cosmetic Co.,Ltd. (420020595) Establishment Name Address ID/FEI Business Operations Guangzhou BEAVER Cosmetic Co.,Ltd. 420020595 manufacture(74159-004)