NDC 69244-0007 Dr.forhair Folligen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 69244-0007?
What are the uses for Dr.forhair Folligen?
Which are Dr.forhair Folligen UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Dr.forhair Folligen 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)
- DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)
- LAURYL HYDROXYSULTAINE (UNII: 176KKP31OZ)
- COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
- STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)
- PEG-120 METHYL GLUCOSE DIOLEATE (UNII: YM0K64F20V)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM LAUROYL METHYLAMINOPROPIONATE (UNII: 99E3R68Y9B)
- ALCOHOL (UNII: 3K9958V90M)
- PEG-45 PALM KERNEL GLYCERIDES (UNII: UC117W498W)
- PANTHENOL (UNII: WV9CM0O67Z)
- C12-13 ALKYL LACTATE (UNII: 9GLX7JL13M)
- CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TRIHYDROXYSTEARIN (UNII: 06YD7896S3)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".