Label: HAND SANITIZER- hand sanitizer spray spray
-
Contains inactivated NDC Code(s)
NDC Code(s): 74881-005-01, 74881-005-02 - Packager: Huizhou Baozi Biotechnology 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 January 6, 2021
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Uses
-
Warnings
Warnings. Flammable. Keep away from fire or flame For extend use or When using this product do not use in or near the eyes. in case of contact, rinse eyes thoroughly with water. stop use and ask a doctor if imitation or rash appears and lasts. Keep out of reach of children. I swallowed, get medical help or contact a Poison Control Center immediately
- DO NOT USE
- WHEN USING THIS PRODUCT
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
HAND SANITIZER
hand sanitizer spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74881-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength CAPRYLYL GLYCOL (UNII: 00YIU5438U) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) WATER (UNII: 059QF0KO0R) ISOPROPYL ALCOHOL (UNII: ND2M416302) 1-AMINOBUTAN-2-OL (UNII: 19453GN3YQ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74881-005-01 150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/23/2020 2 NDC:74881-005-02 150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 06/23/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/23/2020 Labeler - Huizhou Baozi Biotechnology Co., Ltd. (419304583) Registrant - Huizhou Baozi Biotechnology Co., Ltd. (419304583) Establishment Name Address ID/FEI Business Operations Huizhou Baozi Biotechnology Co., Ltd. 419304583 manufacture(74881-005)