NDC 63083-2086 Cerebral Blood Stim Drops 2086
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-2086 - Cerebral Blood Stim Drops
Product Packages
NDC Code 63083-2086-2
Package Description: 59 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-2086?
What are the uses for Cerebral Blood Stim Drops 2086?
Which are Cerebral Blood Stim Drops 2086 UNII Codes?
The UNII codes for the active ingredients in this product are:
- GINKGO (UNII: 19FUJ2C58T)
- GINKGO (UNII: 19FUJ2C58T) (Active Moiety)
- SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC)
- SCUTELLARIA LATERIFLORA WHOLE (UNII: 7BP4DH5PDC) (Active Moiety)
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE)
- CONVALLARIA MAJALIS (UNII: QHH4HVF5QE) (Active Moiety)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
- BOS TAURUS BRAIN (UNII: A1YEE2DB8Z)
- BOS TAURUS BRAIN (UNII: A1YEE2DB8Z) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL)
- HUMAN HERPESVIRUS 1 (UNII: 22G38P19RL) (Active Moiety)
- HYDROGEN CYANIDE (UNII: 2WTB3V159F)
- HYDROGEN CYANIDE (UNII: 2WTB3V159F) (Active Moiety)
Which are Cerebral Blood Stim Drops 2086 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)
- WATER (UNII: 059QF0KO0R)
* 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".