NDC 77388-003 Zuum Klin 63 Ethyl Alcohol Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 77388 - U.s. Cotton Mexico, S. De R.l. De C.v.
- 77388-003 - Zuum Klin 63 Ethyl Alcohol Hand Sanitizer
Product Packages
NDC Code 77388-003-01
Package Description: 60 mL in 1 BOTTLE
NDC Code 77388-003-02
Package Description: 2000 mL in 1 BOTTLE
Product Details
What is NDC 77388-003?
What are the uses for Zuum Klin 63 Ethyl Alcohol Hand Sanitizer?
Which are Zuum Klin 63 Ethyl Alcohol Hand Sanitizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Zuum Klin 63 Ethyl Alcohol Hand Sanitizer 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:
- WATER (UNII: 059QF0KO0R)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- LEMON (UNII: 24RS0A988O)
- EDETIC ACID (UNII: 9G34HU7RV0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
What is the NDC to RxNorm Crosswalk for Zuum Klin 63 Ethyl Alcohol Hand Sanitizer?
- RxCUI: 1094724 - ethanol 63 % Topical Gel
- RxCUI: 1094724 - ethanol 0.63 ML/ML Topical Gel
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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".