NDC 58194-030 Advanced Acne Spot Treatment
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58194 - Shanghai Weierya Daily Chemicals Factory
- 58194-030 - Advanced Acne Spot Treatment
Product Packages
NDC Code 58194-030-01
Package Description: 1 TUBE in 1 CARTON / 21 g in 1 TUBE
Product Details
What is NDC 58194-030?
What are the uses for Advanced Acne Spot Treatment?
Which are Advanced Acne Spot 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 Advanced Acne Spot 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:
- ALCOHOL (UNII: 3K9958V90M)
- AMMONIA (UNII: 5138Q19F1X)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- HAMAMELIS VIRGINIANA TOP (UNII: UDA30A2JJY)
- LAURETH-7 (UNII: Z95S6G8201)
- METHYL LACTATE, (-)- (UNII: 0379G9C44S)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)
- PURSLANE (UNII: M6S840WXG5)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Advanced Acne Spot Treatment?
- RxCUI: 346298 - salicylic acid 2 % Topical Gel
- RxCUI: 346298 - salicylic acid 0.02 MG/MG Topical Gel
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[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".