NDC 81277-102 Zest Hand Sanitizer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 81277 - Tcp Hrb Holdings Llc
- 81277-102 - Zest Hand Sanitizer
Product Packages
NDC Code 81277-102-08
Package Description: 236 mL in 1 BOTTLE
Product Details
What is NDC 81277-102?
What are the uses for Zest Hand Sanitizer?
Which are Zest 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 Zest 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)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERIN (UNII: PDC6A3C0OX)
- AGASTACHE FOENICULUM WHOLE (UNII: ZV7TA06J2V)
- AGAVE TEQUILANA LEAF (UNII: 05545M0E3M)
- LEMON PEEL (UNII: 72O054U628)
- COFFEE BEAN (UNII: JFH385Y744)
- MALPIGHIA GLABRA FRUIT (UNII: B94O42LA9M)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- MALIC ACID (UNII: 817L1N4CKP)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Zest Hand Sanitizer?
- RxCUI: 581662 - ethanol 70 % Topical Gel
- RxCUI: 581662 - ethanol 0.7 ML/ML Topical Gel
- RxCUI: 581662 - ethyl alcohol 70 % Topical Gel
* Please review the disclaimer below.
[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".