NDC 73517-812 Olika Hydrating Hand Sanitizer, Sugar Plum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73517 - Amyris, Inc
- 73517-812 - Olika Hydrating Hand Sanitizer, Sugar Plum
Product Packages
NDC Code 73517-812-02
Package Description: 20 mL in 1 BOTTLE, DISPENSING
NDC Code 73517-812-03
Package Description: 90 mL in 1 POUCH
Product Details
What is NDC 73517-812?
What are the uses for Olika Hydrating Hand Sanitizer, Sugar Plum?
Which are Olika Hydrating Hand Sanitizer, Sugar Plum UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Olika Hydrating Hand Sanitizer, Sugar Plum 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:
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- FRAGRANCE 13576 (UNII: 5EM498GW35)
- TERT-BUTYL ALCOHOL (UNII: MD83SFE959)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- DENATONIUM BENZOATE (UNII: 4YK5Z54AT2)
What is the NDC to RxNorm Crosswalk for Olika Hydrating Hand Sanitizer, Sugar Plum?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".