NDC 68343-005 Dermisa Skin Fade Vitamin C Infused
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 68343-005?
What are the uses for Dermisa Skin Fade Vitamin C Infused?
Which are Dermisa Skin Fade Vitamin C Infused UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Dermisa Skin Fade Vitamin C Infused 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:
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- SULFITE ION (UNII: 15744271E9)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- HYDROXYCITRONELLOL (UNII: R0B4U2I48W)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- PETROLATUM (UNII: 4T6H12BN9U)
- STEARETH-10 (UNII: FD0913P475)
- STEARETH-2 (UNII: V56DFE46J5)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
What is the NDC to RxNorm Crosswalk for Dermisa Skin Fade Vitamin C Infused?
- RxCUI: 153031 - hydroquinone 2 % Topical Cream
- RxCUI: 153031 - hydroquinone 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".