NDC 63083-9244 Secale Combination 9244
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63083 - Professional Complementary Health Formulas
- 63083-9244 - Secale Combination
Product Packages
NDC Code 63083-9244-1
Package Description: 29.5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 63083-9244?
What are the uses for Secale Combination 9244?
Which are Secale Combination 9244 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)
- CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N) (Active Moiety)
- SOLANUM NIGRUM TOP (UNII: O4G5C1G3W5)
- SOLANUM NIGRUM TOP (UNII: O4G5C1G3W5) (Active Moiety)
- AVISCUMINE (UNII: 4B18YVW82N)
- AVISCUMINE (UNII: 4B18YVW82N) (Active Moiety)
- SILVER NITRATE (UNII: 95IT3W8JZE)
- SILVER CATION (UNII: 57N7B0K90A) (Active Moiety)
- BARIUM IODIDE (UNII: WKC4T7680A)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- TOBACCO LEAF (UNII: 6YR2608RSU)
- TOBACCO LEAF (UNII: 6YR2608RSU) (Active Moiety)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
Which are Secale Combination 9244 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".