NDC 44911-0613 Male Balance
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 44911-0613?
What are the uses for Male Balance?
Which are Male Balance UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- PORK LIVER (UNII: 6EC706HI7F)
- PORK LIVER (UNII: 6EC706HI7F) (Active Moiety)
- SUS SCROFA TESTICLE (UNII: KM02613O28)
- SUS SCROFA TESTICLE (UNII: KM02613O28) (Active Moiety)
- TESTOSTERONE (UNII: 3XMK78S47O)
- TESTOSTERONE (UNII: 3XMK78S47O) (Active Moiety)
- CHASTE TREE (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79)
- SUS SCROFA HYPOTHALAMUS (UNII: N6R0856Z79) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SOMATROPIN (UNII: NQX9KB6PCL)
- SOMATROPIN (UNII: NQX9KB6PCL) (Active Moiety)
- EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89)
- EPIMEDIUM GRANDIFLORUM TOP (UNII: 137PC46F89) (Active Moiety)
- SEROTONIN HYDROCHLORIDE (UNII: GKN429M9VS)
- SEROTONIN (UNII: 333DO1RDJY) (Active Moiety)
Which are Male Balance 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- WATER (UNII: 059QF0KO0R)
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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".