NDC 43772-0005 Oligo Iodine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 43772-0005?
What are the uses for Oligo Iodine?
Which are Oligo Iodine UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN)
- CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (Active Moiety)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID)
- SPONGIA OFFICINALIS SKELETON, ROASTED (UNII: 1PIP394IID) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T)
- GERMANIUM SESQUIOXIDE (UNII: 96WE91N25T) (Active Moiety)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- FERROUS IODIDE (UNII: F5452U54PN)
- FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- PULSATILLA VULGARIS (UNII: I76KB35JEV)
- PULSATILLA VULGARIS (UNII: I76KB35JEV) (Active Moiety)
- CYSTEINE (UNII: K848JZ4886)
- CYSTEINE (UNII: K848JZ4886) (Active Moiety)
- SODIUM DIETHYL OXALACETATE (UNII: 6CA025Y4FG)
- DIETHYL OXALACETATE (UNII: 15S56468G7) (Active Moiety)
- FUMARIC ACID (UNII: 88XHZ13131)
- FUMARIC ACID (UNII: 88XHZ13131) (Active Moiety)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X)
- .ALPHA.-KETOGLUTARIC ACID (UNII: 8ID597Z82X) (Active Moiety)
- MANGANESE GLUCONATE (UNII: 9YY2F980SV)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K)
- BOS TAURUS PITUITARY GLAND (UNII: 7JM57I419K) (Active Moiety)
- GOLD (UNII: 79Y1949PYO)
- GOLD (UNII: 79Y1949PYO) (Active Moiety)
- MOLYBDENUM (UNII: 81AH48963U)
- MOLYBDENUM (UNII: 81AH48963U) (Active Moiety)
- PALLADIUM (UNII: 5TWQ1V240M)
- PALLADIUM (UNII: 5TWQ1V240M) (Active Moiety)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2)
- MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (Active Moiety)
- SILVER (UNII: 3M4G523W1G)
- SILVER (UNII: 3M4G523W1G) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- ZINC (UNII: J41CSQ7QDS)
- ZINC (UNII: J41CSQ7QDS) (Active Moiety)
- COPPER (UNII: 789U1901C5)
- COPPER (UNII: 789U1901C5) (Active Moiety)
- NICKEL (UNII: 7OV03QG267)
- NICKEL (UNII: 7OV03QG267) (Active Moiety)
- EUGENOL (UNII: 3T8H1794QW)
- EUGENOL (UNII: 3T8H1794QW) (Active Moiety)
- FORMALDEHYDE (UNII: 1HG84L3525)
- FORMALDEHYDE (UNII: 1HG84L3525) (Active Moiety)
- TITANIUM (UNII: D1JT611TNE)
- TITANIUM (UNII: D1JT611TNE) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- RANCID BEEF (UNII: 29SUH5R3HU)
- RANCID BEEF (UNII: 29SUH5R3HU) (Active Moiety)
- VANADIUM (UNII: 00J9J9XKDE)
- VANADIUM (UNII: 00J9J9XKDE) (Active Moiety)
- BROMINE (UNII: SBV4XY874G)
- BROMINE (UNII: SBV4XY874G) (Active Moiety)
- CALCIUM IODIDE (UNII: 8EKI9QEE2H)
- CALCIUM CATION (UNII: 2M83C4R6ZB) (Active Moiety)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN)
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED (UNII: U364V64HUN) (Active Moiety)
- HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD)
- HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD) (Active Moiety)
Which are Oligo Iodine 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".