NDC 63776-081 Viatrexx-cellulite
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 63776-081?
What are the uses for Viatrexx-cellulite?
Which are Viatrexx-cellulite UNII Codes?
The UNII codes for the active ingredients in this product are:
- ANDROSTERONE (UNII: C24W7J5D5R)
- ANDROSTERONE (UNII: C24W7J5D5R) (Active Moiety)
- ARTICHOKE (UNII: 4F3W47PLBE)
- ARTICHOKE (UNII: 4F3W47PLBE) (Active Moiety)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
- BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V) (Active Moiety)
- ERSOFERMIN (UNII: 1NWT5SW3NW)
- ERSOFERMIN (UNII: 1NWT5SW3NW) (Active Moiety)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (Active Moiety)
- LEVOCARNITINE (UNII: 0G389FZZ9M)
- LEVOCARNITINE (UNII: 0G389FZZ9M) (Active Moiety)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- CENTELLA ASIATICA (UNII: 7M867G6T1U) (Active Moiety)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) (Active Moiety)
- COBALT (UNII: 3G0H8C9362)
- COBALT (UNII: 3G0H8C9362) (Active Moiety)
- ESTROGENS, ESTERIFIED (UNII: 3ASP8Q3768)
- ESTROGENS, ESTERIFIED (UNII: 3ASP8Q3768) (Active Moiety)
- FERROUS FUMARATE (UNII: R5L488RY0Q)
- FERROUS CATION (UNII: GW89581OWR) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- HEPTAMINOL (UNII: 3DQS188SY5)
- HEPTAMINOL (UNII: 3DQS188SY5) (Active Moiety)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY)
- HAMAMELIS VIRGINIANA BARK (UNII: IH3063S9MY) (Active Moiety)
- HYALURONIDASE (UNII: 8KOG53Z5EM)
- HYALURONIDASE (UNII: 8KOG53Z5EM) (Active Moiety)
- INTERLEUKIN-3 (UNII: A802907MI4)
- INTERLEUKIN-3 (UNII: A802907MI4) (Active Moiety)
- POTASSIUM ASPARTATE (UNII: OC4598NZEQ)
- ASPARTIC ACID (UNII: 30KYC7MIAI) (Active Moiety)
- LACTIC ACID (UNII: 33X04XA5AT)
- LACTIC ACID (UNII: 33X04XA5AT) (Active Moiety)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV)
- BOS TAURUS LYMPH VESSEL (UNII: 85I1Z426OV) (Active Moiety)
- SUS SCROFA LYMPH VESSEL (UNII: SFL7R07748)
- SUS SCROFA LYMPH VESSEL (UNII: SFL7R07748) (Active Moiety)
- MELILOTUS OFFICINALIS WHOLE (UNII: DJR90OLD7P)
- MELILOTUS OFFICINALIS WHOLE (UNII: DJR90OLD7P) (Active Moiety)
- MANGANESE (UNII: 42Z2K6ZL8P)
- MANGANESE (UNII: 42Z2K6ZL8P) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- SODIUM PYRUVATE (UNII: POD38AIF08)
- PYRUVIC ACID (UNII: 8558G7RUTR) (Active Moiety)
- QUINHYDRONE (UNII: P4A66LQ3QJ)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
- SUCCINIC ACID (UNII: AB6MNQ6J6L)
- SUCCINIC ACID (UNII: AB6MNQ6J6L) (Active Moiety)
- BOS TAURUS VEIN (UNII: 3H31IR83LT)
- BOS TAURUS VEIN (UNII: 3H31IR83LT) (Active Moiety)
- SUS SCROFA VEIN (UNII: 2510RH3I89)
- SUS SCROFA VEIN (UNII: 2510RH3I89) (Active Moiety)
- VITAMIN A (UNII: 81G40H8B0T)
- VITAMIN A (UNII: 81G40H8B0T) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
Which are Viatrexx-cellulite 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".