NDC 58133-500 Nuvileo Skin Perfecting Acne
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 58133-500?
What are the uses for Nuvileo Skin Perfecting Acne?
Which are Nuvileo Skin Perfecting Acne UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Nuvileo Skin Perfecting Acne 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ALOE VERA WHOLE (UNII: KIZ4X2EHYX)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- HYDRASTIS CANADENSIS WHOLE (UNII: R763EBH88T)
- LAURETH-7 (UNII: Z95S6G8201)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- PANAX QUINQUEFOLIUS WHOLE (UNII: 0P067WOA1X)
- PASSIFLORA INCARNATA FLOWERING TOP (UNII: CLF5YFS11O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Nuvileo Skin Perfecting Acne?
- RxCUI: 1658308 - Nuvileo 2 % Topical Cream
- RxCUI: 1658308 - salicylic acid 20 MG/ML Topical Cream [Nuvileo]
- RxCUI: 317152 - salicylic acid 2 % Topical Cream
- RxCUI: 317152 - salicylic acid 20 MG/ML Topical Cream
* 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".