NDC 55118-532 Scott Moisturizing Foam Hand Sanitizer (ultra)
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55118 - Kimberly-clark
- 55118-532 - Scott Moisturizing Foam Hand Sanitizer (ultra)
Product Packages
NDC Code 55118-532-63
Package Description: 6 BOTTLE in 1 CARTON / 1000 mL in 1 BOTTLE (55118-532-10)
NDC Code 55118-532-65
Package Description: 2 BOTTLE in 1 CARTON / 1200 mL in 1 BOTTLE (55118-532-12)
Product Details
What is NDC 55118-532?
What are the uses for Scott Moisturizing Foam Hand Sanitizer (ultra)?
Which are Scott Moisturizing Foam Hand Sanitizer (ultra) UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Scott Moisturizing Foam Hand Sanitizer (ultra) Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
What is the NDC to RxNorm Crosswalk for Scott Moisturizing Foam Hand Sanitizer (ultra)?
- RxCUI: 616805 - ethanol 70 % Topical Foam
- RxCUI: 616805 - ethanol 0.7 ML/ML Topical Foam
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".