NDC 51830-053 Cleansing Foaming Gel Acne Pro Skin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 51830-053?
What are the uses for Cleansing Foaming Gel Acne Pro Skin?
Which are Cleansing Foaming Gel Acne Pro Skin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC PIDOLATE (UNII: C32PQ86DH4)
- ZINC PIDOLATE (UNII: C32PQ86DH4) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD)
- IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD) (Active Moiety)
Which are Cleansing Foaming Gel Acne Pro Skin 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)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- ZINC ACETYLMETHIONATE (UNII: Q98AWH82LP)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- HEDERA HELIX LEAF (UNII: ZP9XFG71A7)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ALCOHOL (UNII: 3K9958V90M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- FYTIC ACID (UNII: 7IGF0S7R8I)
- BIOTIN (UNII: 6SO6U10H04)
- TROLAMINE (UNII: 9O3K93S3TK)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- HYDROXYISOHEXYL 3-CYCLOHEXENE CARBOXALDEHYDE (UNII: QUE43B9Z2Q)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ETHYLPARABEN (UNII: 14255EXE39)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
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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".