NDC 62499-392 Clear Up Control Solution Anti-blemiches
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62499-392?
What are the uses for Clear Up Control Solution Anti-blemiches?
Which are Clear Up Control Solution Anti-blemiches 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 Clear Up Control Solution Anti-blemiches 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)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- AMYLOPECTIN (UNII: 4XO4QFV777)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- LACTIC ACID (UNII: 33X04XA5AT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ARGININE (UNII: 94ZLA3W45F)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALLANTOIN (UNII: 344S277G0Z)
- ORANGE OIL (UNII: AKN3KSD11B)
- ALMOND OIL (UNII: 66YXD4DKO9)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- SAGE OIL (UNII: U27K0H1H2O)
- LAVANDIN OIL (UNII: 9RES347CKG)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CHAMOMILE FLOWER OIL (UNII: 60F80Z61A9)
What is the NDC to RxNorm Crosswalk for Clear Up Control Solution Anti-blemiches?
- RxCUI: 251577 - salicylic acid 2 % Topical Solution
- RxCUI: 251577 - salicylic acid 20 MG/ML Topical Solution
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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".