NDC 52731-7036 Male Complex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52731 - Nova Homeopathic Therapeutics, Inc.
- 52731-7036 - Male Complex
Product Packages
NDC Code 52731-7036-2
Package Description: 1 BOTTLE in 1 BOX / 50 mL in 1 BOTTLE (52731-7036-1)
Product Details
What is NDC 52731-7036?
What are the uses for Male Complex?
Which are Male Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- LYTTA VESICATORIA (UNII: 3Q034RO3BT)
- LYTTA VESICATORIA (UNII: 3Q034RO3BT) (Active Moiety)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J) (Active Moiety)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z)
- CHONDRODENDRON TOMENTOSUM ROOT (UNII: 395A3P448Z) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- SAW PALMETTO (UNII: J7WWH9M8QS)
- SAW PALMETTO (UNII: J7WWH9M8QS) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
Which are Male Complex 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)
* 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".