NDC 70827-001 Antibacterial Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70827 - Top Trenz
- 70827-001 - Antibacterial Hand Sanitizer
Product Packages
NDC Code 70827-001-01
Package Description: 29 mL in 1 BOTTLE
Product Details
What is NDC 70827-001?
What are the uses for Antibacterial Hand Sanitizer?
Which are Antibacterial 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 Antibacterial 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- LACTOSE (UNII: J2B2A4N98G)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- ULTRAMARINE BLUE (UNII: I39WR998BI)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
What is the NDC to RxNorm Crosswalk for Antibacterial Hand Sanitizer?
- RxCUI: 581660 - ethanol 62 % Topical Gel
- RxCUI: 581660 - ethanol 0.62 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".