Label: FA HAND SANITIZER GEL 70% (ETHANOL)- hand sanitizer gel
- NDC Code(s): 74932-100-01
- Packager: HLB CO.,LTD_Healthcare
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 7, 2024
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
- When useing this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive Ingredients
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
FA HAND SANITIZER GEL 70% (ETHANOL)
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74932-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74932-100-01 1 in 1 BOX 04/10/2020 1 57 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 04/10/2020 Labeler - HLB CO.,LTD_Healthcare (987587913) Registrant - HLB CO.,LTD_Healthcare (987587913) Establishment Name Address ID/FEI Business Operations HLB CO.,LTD_Healthcare 987587913 manufacture(74932-100)