Label: KLEENEX INSTANT HAND SANITIZER- alcohol solution
- NDC Code(s): 55118-704-70, 55118-704-88
- Packager: Kimberly-Clark Corporation
- 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 July 13, 2023
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
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- Inactive Ingredients
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label
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INGREDIENTS AND APPEARANCE
KLEENEX INSTANT HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-704 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 68 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-704-70 6 in 1 CARTON 08/30/2021 1 NDC:55118-704-88 236 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333E 08/30/2021 Labeler - Kimberly-Clark Corporation (830997032)