NDC 58876-105 Acne Cleansing Wipes
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58876 - Dr Lin Skincare
- 58876-105 - Acne Cleansing Wipes
Product Packages
NDC Code 58876-105-01
Package Description: 1 LIQUID in 1 POUCH
NDC Code 58876-105-10
Package Description: 10 LIQUID in 1 POUCH
NDC Code 58876-105-35
Package Description: 35 LIQUID in 1 POUCH
Product Details
What is NDC 58876-105?
What are the uses for Acne Cleansing Wipes?
Which are Acne Cleansing Wipes 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 Acne Cleansing Wipes 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- WITCH HAZEL (UNII: 101I4J0U34)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- MENTHOL (UNII: L7T10EIP3A)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Acne Cleansing Wipes?
- RxCUI: 797892 - salicylic acid 2 % Medicated Pad
- RxCUI: 797892 - salicylic acid 20 MG/ML Medicated Pad
- RxCUI: 797892 - salicylic acid 2 % Topical Swab
* 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".