NDC 65903-272 Anti Acne Calming Corrector
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 65903-272?
What are the uses for Anti Acne Calming Corrector?
Which are Anti Acne Calming Corrector 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 Anti Acne Calming Corrector 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)
- ALCOHOL (UNII: 3K9958V90M)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- LINOLEAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: 5Q87K461JO)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SEA SALT (UNII: 87GE52P74G)
- DULSE (UNII: 7832HOY4ZQ)
- CRITHMUM MARITIMUM (UNII: J7IHY79BKY)
- HIMANTHALIA ELONGATA (UNII: 21RND18XRR)
- MASTOCARPUS STELLATUS (UNII: 6T087FC66H)
- MACROCYSTIS PYRIFERA (UNII: K31S3OG5C4)
- ZINC SULFATE (UNII: 89DS0H96TB)
What is the NDC to RxNorm Crosswalk for Anti Acne Calming Corrector?
- RxCUI: 416212 - salicylic acid 1.5 % Topical Gel
- RxCUI: 416212 - salicylic acid 0.015 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".