NDC 80457-002 Anti-bacter Hand Sanitizer 70 Ethyl Alcohol Coconut
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 80457 - Adex Cosmetics & Pharma Leszek Sierdzinski
- 80457-002 - Anti-bacter Hand Sanitizer 70 Ethyl Alcohol Coconut
Product Packages
NDC Code 80457-002-01
Package Description: 100 mL in 1 BOTTLE
Product Details
What is NDC 80457-002?
What are the uses for Anti-bacter Hand Sanitizer 70 Ethyl Alcohol Coconut?
Which are Anti-bacter Hand Sanitizer 70 Ethyl Alcohol Coconut UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Anti-bacter Hand Sanitizer 70 Ethyl Alcohol Coconut 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- MANNITOL (UNII: 3OWL53L36A)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Anti-bacter Hand Sanitizer 70 Ethyl Alcohol Coconut?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % 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".