NDC 80761-001 Skininc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 80761-001?
What are the uses for Skininc?
Which are Skininc UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALCOHOL (UNII: 3K9958V90M)
- ALCOHOL (UNII: 3K9958V90M) (Active Moiety)
Which are Skininc 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)
- MANNITOL (UNII: 3OWL53L36A)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- MENTHA X ROTUNDIFOLIA LEAF (UNII: K59TXG2L3U)
- MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9)
- MENTHA AQUATICA LEAF (UNII: 5M106ME6PT)
- PUMPKIN (UNII: SYW0QUB89Y)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- ANGELICA GIGAS ROOT (UNII: 32766B2FHX)
- CNIDIUM OFFICINALE ROOT (UNII: 8S3OZD358J)
- MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)
What is the NDC to RxNorm Crosswalk for Skininc?
- RxCUI: 902574 - ethanol 65 % Topical Gel
- RxCUI: 902574 - ethanol 0.65 ML/ML Topical Gel
- RxCUI: 902574 - ethyl alcohol 65 % 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".