Label: SCOTT MOISTURIZING FOAM HAND SANITIZER (ULTRA)- alcohol solution
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Contains inactivated NDC Code(s)
NDC Code(s): 55118-532-10, 55118-532-12, 55118-532-63, 55118-532-65 - Packager: Kimberly-Clark
- 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 October 18, 2019
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Directions
- Other Information
- Inactive Ingredients
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- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 33.8 fl oz Bottle Label
34700
SAME GREAT
FORMULATION.
Now Scott®
branded!Scott®
BrandMoisturizing
Foam Hand SanitizerULTRA
Leave OnEmpty &
Discard Pump
PLASTIC
BOTTLE20-14-658-0-03
how2recycle.info
ECOLOGO
PRODUCT CERTIFIED FOR
REDUCED ENVIRONMENTAL
IMPACT. VIEW SPECIFIC
ATTRIBUTES EVAUATED:
UL.COM/EL UL 2783NPN: 80030706
For Personal / Domestic Use Only
1 Liter (33.8 fl oz)
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INGREDIENTS AND APPEARANCE
SCOTT MOISTURIZING FOAM HAND SANITIZER (ULTRA)
alcohol solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55118-532 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 ALOE VERA LEAF (UNII: ZY81Z83H0X) Betaine (UNII: 3SCV180C9W) GREEN TEA LEAF (UNII: W2ZU1RY8B0) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) CUCUMBER (UNII: YY7C30VXJT) Glycerin (UNII: PDC6A3C0OX) ISOPROPYL ALCOHOL (UNII: ND2M416302) MEADOWFOAMAMIDOPROPYL BETAINE (UNII: HNV0L650LG) Panthenol (UNII: WV9CM0O67Z) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55118-532-63 6 in 1 CARTON 04/25/2018 1 NDC:55118-532-10 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:55118-532-65 2 in 1 CARTON 04/25/2018 2 NDC:55118-532-12 1200 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 04/25/2018 Labeler - Kimberly-Clark (830997032)