NDC 43857-0513 Occuloplex G
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43857 - Bioactive Nutritional, Inc.
- 43857-0513 - Occuloplex G
Product Packages
NDC Code 43857-0513-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43857-0513?
What are the uses for Occuloplex G?
Which are Occuloplex G UNII Codes?
The UNII codes for the active ingredients in this product are:
- EUPHRASIA STRICTA (UNII: C9642I91WL)
- EUPHRASIA STRICTA (UNII: C9642I91WL) (Active Moiety)
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX)
- PETROSELINUM CRISPUM (UNII: 1WZA4Y92EX) (Active Moiety)
- BILBERRY (UNII: 9P2U39H18W)
- BILBERRY (UNII: 9P2U39H18W) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE)
- SPIGELIA ANTHELMIA (UNII: WYT05213GE) (Active Moiety)
- SUS SCROFA EYE (UNII: X3AOK514E6)
- SUS SCROFA EYE (UNII: X3AOK514E6) (Active Moiety)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
- UBIDECARENONE (UNII: EJ27X76M46)
- UBIDECARENONE (UNII: EJ27X76M46) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q)
- CALCIUM SULFIDE (UNII: 1MBW07J51Q) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S)
- RUTA GRAVEOLENS FLOWERING TOP (UNII: N94C2U587S) (Active Moiety)
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
- LITHIUM (UNII: 9FN79X2M3F)
- LITHIUM CATION (UNII: 8H8Z5UER66) (Active Moiety)
Which are Occuloplex G 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".