NDC 81653-008 Regenivade Hair Growth Foam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 81653-008?
What are the uses for Regenivade Hair Growth Foam?
Which are Regenivade Hair Growth Foam UNII Codes?
The UNII codes for the active ingredients in this product are:
- MINOXIDIL (UNII: 5965120SH1)
- MINOXIDIL (UNII: 5965120SH1) (Active Moiety)
Which are Regenivade Hair Growth Foam 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:
- VITIS VINIFERA POLLEN (UNII: 83OVS854BE)
- WATER (UNII: 059QF0KO0R)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- ROSEMARY OIL (UNII: 8LGU7VM393)
- URTICA DIOICA (UNII: 710FLW4U46)
- POLYGONUM CUSPIDATUM LEAF (UNII: 2540B7G25G)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- BIOTIN (UNII: 6SO6U10H04)
- JOJOBA OIL (UNII: 724GKU717M)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- N-ETHYLHEXEDRONE (UNII: TAX3KSX6GY)
- HYALURONIC ACID (UNII: S270N0TRQY)
- GLYOXYLOYL CARBOCYSTEINE (UNII: 3K6008UJ5J)
- ALLANTOIN (UNII: 344S277G0Z)
- PUMPKIN SEED OIL (UNII: 6E5QR5USSP)
- CAFFEINE (UNII: 3G6A5W338E)
- NIACIN (UNII: 2679MF687A)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- XANTHAN GUM (UNII: TTV12P4NEE)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- ARGAN OIL (UNII: 4V59G5UW9X)
- CASTOR OIL (UNII: D5340Y2I9G)
- AMINO ACIDS, HAIR KERATIN (UNII: G46579QK1M)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
What is the NDC to RxNorm Crosswalk for Regenivade Hair Growth Foam?
- 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
* Please review the disclaimer below.
[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".