Label: KLEENEX ULTRA MOISTURIZING HAND SANITIZER- alcohol solution
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NDC Code(s):
55118-530-10,
55118-530-11,
55118-530-12,
55118-530-88, view more55118-530-99
- Packager: Kimberly-Clark Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 10, 2024
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Uses
- Warnings
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- Other information
- Inactive Ingredients
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- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 1L Bottle Label
34700
Kleenex®
BRAND MARQUE
ULTRAMoisturizing Foam
Hand SanitizerSAME GREAT FORMULATION.
Now Kleenex® BrandedFor Personal / Domestic Use Only
1L (33.8 fl oz)
Empty &
Discard Pump
PLASTIC
BOTTLEhow2recycle.info
NPN 80030706
ECOLOGO
PRODUCT CERTIFIED FOR
REDUCED ENVIRONMENTAL
IMPACT. VIEW SPECIFIC
ATTRIBUTES EVAUATED:
UL.COM/EL UL 278420-14-833-0-00
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INGREDIENTS AND APPEARANCE
KLEENEX ULTRA MOISTURIZING HAND SANITIZER
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-530 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 Water (UNII: 059QF0KO0R) Isopropyl Alcohol (UNII: ND2M416302) Betaine (UNII: 3SCV180C9W) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) GREEN TEA LEAF (UNII: W2ZU1RY8B0) Panthenol (UNII: WV9CM0O67Z) Glycerin (UNII: PDC6A3C0OX) MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG) Aloe Vera Leaf (UNII: ZY81Z83H0X) Cucumber (UNII: YY7C30VXJT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-530-88 236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2012 2 NDC:55118-530-99 472 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2012 3 NDC:55118-530-11 44 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 03/01/2012 4 NDC:55118-530-10 1000 mL in 1 BAG; Type 0: Not a Combination Product 03/01/2012 5 NDC:55118-530-12 1200 mL in 1 BAG; Type 0: Not a Combination Product 03/01/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph drug M003 03/01/2012 Labeler - Kimberly-Clark Corporation (830997032) Establishment Name Address ID/FEI Business Operations Tri-Pac Inc. 020844956 MANUFACTURE(55118-530) , LABEL(55118-530) , PACK(55118-530) Establishment Name Address ID/FEI Business Operations Cyan Labs 812754130 MANUFACTURE(55118-530) , LABEL(55118-530) , ANALYSIS(55118-530) , PACK(55118-530)