Label: SUAVE- hand sanitizer gel
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1744-1 - Packager: Conopco Inc. d/b/a/ Unilever
- 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 December 7, 2022
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- Official Label (Printer Friendly)
- SUAVE HAND SANITIZER - Ethyl Alcohol gel
- Drug Facts
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- Questions?
- Packaging
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INGREDIENTS AND APPEARANCE
SUAVE
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1744 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 700 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1744-1 88 mL in 1 TUBE; Type 0: Not a Combination Product 06/15/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 06/15/2020 Labeler - Conopco Inc. d/b/a/ Unilever (001375088)