NDC 43857-0363 Orchiforce
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0363 - Orchiforce
Product Packages
NDC Code 43857-0363-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0363?
What are the uses for Orchiforce?
Which are Orchiforce 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)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ)
- TURNERA DIFFUSA LEAFY TWIG (UNII: RQ2CFA7WWJ) (Active Moiety)
- CHASTE TREE (UNII: 433OSF3U8A)
- CHASTE TREE (UNII: 433OSF3U8A) (Active Moiety)
- DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B)
- DIEFFENBACHIA SEGUINE (UNII: 01800C6E6B) (Active Moiety)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371)
- CONIUM MACULATUM FLOWERING TOP (UNII: Q28R5GF371) (Active Moiety)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- PHOSPHORIC ACID (UNII: E4GA8884NN) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- PICRIC ACID (UNII: A49OS0F91S)
- PICRIC ACID (UNII: A49OS0F91S) (Active Moiety)
Which are Orchiforce 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".