NDC 63776-206 Viatrexx-hair
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63776-206?
What are the uses for Viatrexx-hair?
Which are Viatrexx-hair UNII Codes?
The UNII codes for the active ingredients in this product are:
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- PANTOTHENIC ACID (UNII: 19F5HK2737) (Active Moiety)
- BIOTIN (UNII: 6SO6U10H04)
- BIOTIN (UNII: 6SO6U10H04) (Active Moiety)
- ESTRADIOL (UNII: 4TI98Z838E)
- ESTRADIOL (UNII: 4TI98Z838E) (Active Moiety)
- PORK COLLAGEN (UNII: I8442U2G7J)
- PORK COLLAGEN (UNII: I8442U2G7J) (Active Moiety)
- ESTRIOL (UNII: FB33469R8E)
- ESTRIOL (UNII: FB33469R8E) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- INTERLEUKIN-3 (UNII: A802907MI4)
- INTERLEUKIN-3 (UNII: A802907MI4) (Active Moiety)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
- PROGESTERONE (UNII: 4G7DS2Q64Y)
- PROGESTERONE (UNII: 4G7DS2Q64Y) (Active Moiety)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V) (Active Moiety)
Which are Viatrexx-hair 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:
- ALCOHOL (UNII: 3K9958V90M)
- WATER (UNII: 059QF0KO0R)
* 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".