NDC 73047-004 Skincoach Clean
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73047 - Skin Coach Sl.
- 73047-004 - Skincoach Clean
Product Packages
NDC Code 73047-004-01
Package Description: 200 mL in 1 TUBE
Product Details
What is NDC 73047-004?
What are the uses for Skincoach Clean?
Which are Skincoach Clean 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 Skincoach Clean 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:
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POLY(DL-LACTIC-CO-GLYCOLIC ACID), (50:50; 46000 MW) (UNII: LQ35R50VR1)
- LINOLEAMIDOPROPYL PROPYLENE GLYCOL-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- WATER (UNII: 059QF0KO0R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SODIUM C12-15 PARETH-15 SULFONATE (UNII: 353VA59XH8)
- SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
- TROLAMINE (UNII: 9O3K93S3TK)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- ZINC PIDOLATE (UNII: C32PQ86DH4)
What is the NDC to RxNorm Crosswalk for Skincoach Clean?
- RxCUI: 562600 - salicylic acid 2 % Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 20 MG/ML Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 2 % Facial Cleanser Toner
- RxCUI: 562600 - salicylic acid 2 % Facial Scrub
* 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".