NDC 58990-000 Antiac Acne Clearing
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 58990-000?
What are the uses for Antiac Acne Clearing?
Which are Antiac Acne Clearing 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 Antiac Acne Clearing 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)
- SUNFLOWER SEED OIL GLYCERETH-8 ESTERS (UNII: 358X17CAT0)
- GLYCERYL COCOATE (UNII: WVK1CT5994)
- HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ROSEMARY (UNII: IJ67X351P9)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- TRIDECETH-9 (UNII: X9HD79I514)
- CETEARETH-25 (UNII: 8FA93U5T67)
- ORANGE OIL (UNII: AKN3KSD11B)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Antiac Acne Clearing?
- RxCUI: 1046487 - salicylic acid 0.5 % Topical Spray
- RxCUI: 1046487 - salicylic acid 5 MG/ML Topical Spray
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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".