NDC 81653-009 Profolix Minoxidil Hair Growth Serum
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 81653-009?
What are the uses for Profolix Minoxidil Hair Growth Serum?
Which are Profolix Minoxidil Hair Growth Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINOXIDIL (UNII: 5965120SH1)
- MINOXIDIL (UNII: 5965120SH1) (Active Moiety)
Which are Profolix Minoxidil Hair Growth Serum 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:
- CARTHAMUS TINCTORIUS WHOLE (UNII: 5EMV416J82)
- LIGUSTICUM WALLICHII ROOT (UNII: R81AD159QS)
- GLYCYRRHIZA URALENSIS WHOLE (UNII: 8XW1DS8UIR)
- CAPSAICIN (UNII: S07O44R1ZM)
- BIOTIN (UNII: 6SO6U10H04)
- DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
- ALCOHOL (UNII: 3K9958V90M)
- ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA)
- HOODIA GORDONII SAP (UNII: K7QNF2DJR8)
- WATER (UNII: 059QF0KO0R)
- GINGER (UNII: C5529G5JPQ)
- ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
- REYNOUTRIA MULTIFLORA STEM (UNII: 9V97G011CE)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- LIGUSTRUM LUCIDUM FRUIT (UNII: M9G2U96DUT)
- COLLAGEN ALPHA-1(I) CHAIN BOVINE (UNII: FB3DQM32F2)
What is the NDC to RxNorm Crosswalk for Profolix Minoxidil Hair Growth Serum?
- RxCUI: 311724 - minoxidil 5 % Topical Solution
- RxCUI: 311724 - minoxidil 50 MG/ML Topical Solution
- RxCUI: 311724 - minoxidil 3 GM per 60 ML Topical Solution
- RxCUI: 311724 - minoxidil 5 GM per 100 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".