NDC 58876-104 Dr. Lin Skincare Acne
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58876 - Dr Lin Skincare
- 58876-104 - Dr. Lin Skincare Acne
Product Packages
NDC Code 58876-104-12
Package Description: 60 mL in 1 BOTTLE
Product Details
What is NDC 58876-104?
What are the uses for Dr. Lin Skincare Acne?
Which are Dr. Lin Skincare Acne UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM)
- BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (Active Moiety)
Which are Dr. Lin Skincare 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- ARBUTIN (UNII: C5INA23HXF)
- KOJIC ACID (UNII: 6K23F1TT52)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ALLANTOIN (UNII: 344S277G0Z)
- PANTHENOL (UNII: WV9CM0O67Z)
- GLYCERYL ABIETATE (UNII: 2F22LY70Q1)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Dr. Lin Skincare Acne?
- RxCUI: 200009 - benzoyl peroxide 2.5 % Topical Lotion
- RxCUI: 200009 - benzoyl peroxide 25 MG/ML Topical Lotion
* 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".