NDC 58876-101 Daily Cleanser Salicylic Acid Acne Treatment
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58876-101?
What are the uses for Daily Cleanser Salicylic Acid Acne Treatment?
Which are Daily Cleanser Salicylic Acid Acne 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 Daily Cleanser Salicylic Acid Acne 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)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
- GLYCERIN (UNII: PDC6A3C0OX)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)
- ARBUTIN (UNII: C5INA23HXF)
- KOJIC ACID (UNII: 6K23F1TT52)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- ALLANTOIN (UNII: 344S277G0Z)
- PANTHENOL (UNII: WV9CM0O67Z)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for Daily Cleanser Salicylic Acid Acne Treatment?
- RxCUI: 562600 - salicylic acid 2 % Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 20 MG/ML Medicated Liquid Soap
- RxCUI: 562600 - salicylic acid 2 % Facial Cleanser Toner
- RxCUI: 562600 - salicylic acid 2 % Facial Scrub
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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".