NDC 62839-0390 Nu Skin Clear Action Acne Medication Night Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62839 - Nse Products, Inc.
- 62839-0390 - Nu Skin Clear Action
Product Packages
NDC Code 62839-0390-1
Package Description: 1 TUBE in 1 CARTON / 30 mL in 1 TUBE
Product Details
What is NDC 62839-0390?
What are the uses for Nu Skin Clear Action Acne Medication Night Treatment?
Which are Nu Skin Clear Action Acne Medication Night Treatment 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 Nu Skin Clear Action Acne Medication Night Treatment 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURETH-7 (UNII: Z95S6G8201)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- EDETATE SODIUM (UNII: MP1J8420LU)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Nu Skin Clear Action Acne Medication Night Treatment?
- RxCUI: 1111055 - Nu Skin Clear Action Acne Treatment 0.5 % Topical Gel
- RxCUI: 1111055 - salicylic acid 0.005 MG/MG Topical Gel [Nu Skin Clear Action]
- RxCUI: 1111055 - Nu Skin Clear Action 0.5 % Topical Gel
- RxCUI: 1111055 - Nu Skin Clear Action Day Treatment 0.005 MG/MG Topical Gel
- RxCUI: 252296 - salicylic acid 0.5 % 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".