NDC 50181-0019 Mbm 12 Male
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center For Research And Education
- 50181-0019 - Mbm 12 Male
Product Packages
NDC Code 50181-0019-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 50181-0019?
What are the uses for Mbm 12 Male?
Which are Mbm 12 Male UNII Codes?
The UNII codes for the active ingredients in this product are:
- OXYTOCIN (UNII: 1JQS135EYN)
- OXYTOCIN (UNII: 1JQS135EYN) (Active Moiety)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J)
- CHIMAPHILA UMBELLATA (UNII: WCK21A9W9J) (Active Moiety)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T)
- SUS SCROFA PITUITARY GLAND (UNII: E8S87O660T) (Active Moiety)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36) (Active Moiety)
- SUS SCROFA TESTICLE (UNII: KM02613O28)
- SUS SCROFA TESTICLE (UNII: KM02613O28) (Active Moiety)
- SUS SCROFA PROSTATE (UNII: O6UD3347K2)
- SUS SCROFA PROSTATE (UNII: O6UD3347K2) (Active Moiety)
- SARSAPARILLA (UNII: 2H1576D5WG)
- SARSAPARILLA (UNII: 2H1576D5WG) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- POTASSIUM PHOSPHATE, DIBASIC (UNII: CI71S98N1Z)
- PHOSPHATE ION (UNII: NK08V8K8HR) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
Which are Mbm 12 Male 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:
- WATER (UNII: 059QF0KO0R)
- 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".