NDC 70678-001 Cocoskin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 70678-001?
What are the uses for Cocoskin?
Which are Cocoskin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5)
- PRAMOXINE (UNII: 068X84E056) (Active Moiety)
Which are Cocoskin 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)
- CALCIUM ACETATE (UNII: Y882YXF34X)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- HELIANTHUS ANNUUS WHOLE (UNII: 17S27ZT6KR)
- PETROLATUM (UNII: 4T6H12BN9U)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM DECYLGLUCOSIDE HYDROXYPROPYLSULFONATE (UNII: B306V77S6R)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- ALUMINUM ACETATE (UNII: 80EHD8I43D)
- ALUMINUM SULFATE (UNII: 34S289N54E)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- COCOS NUCIFERA WHOLE (UNII: 245J88W96L)
- SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Cocoskin?
- RxCUI: 1052684 - pramoxine HCl 1 % Topical Cream
- RxCUI: 1052684 - pramoxine hydrochloride 10 MG/ML Topical Cream
- RxCUI: 1052684 - pramoxine hydrochloride 1 % 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".