NDC 69579-106 Phytopecia Hair Tonic
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69579-106?
Which are Phytopecia Hair Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTHENOL (UNII: WV9CM0O67Z)
- PANTHENOL (UNII: WV9CM0O67Z) (Active Moiety)
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
Which are Phytopecia Hair Tonic 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)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PREZATIDE COPPER (UNII: 6BJQ43T1I9)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- MECASERMIN (UNII: 7GR9I2683O)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
- FIBROBLAST GROWTH FACTOR-1 (UNII: G53298VN9Y)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- MENTHOL (UNII: L7T10EIP3A)
- CHAMOMILE (UNII: FGL3685T2X)
- MORUS ALBA BARK (UNII: 7O71A48NDP)
- ROSEMARY (UNII: IJ67X351P9)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- GLUCOSYL HESPERIDIN (UNII: 432C95B6YE)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
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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".