NDC 72866-035 Hand Sanitizer Upside Down
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 72866-035?
What are the uses for Hand Sanitizer Upside Down?
Which are Hand Sanitizer Upside Down UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Hand Sanitizer Upside Down 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:
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- GERANIOL (UNII: L837108USY)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- MANNITOL (UNII: 3OWL53L36A)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SUCROSE (UNII: C151H8M554)
- CORN (UNII: 0N8672707O)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Hand Sanitizer Upside Down?
- RxCUI: 1039708 - ethanol 67 % Topical Gel
- RxCUI: 1039708 - ethanol 0.67 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".