NDC 44911-0309 Thyroid Tonic
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 44911-0309?
What are the uses for Thyroid Tonic?
Which are Thyroid Tonic UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACACIA (UNII: 5C5403N26O)
- ACACIA (UNII: 5C5403N26O) (Active Moiety)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- OLIVE OIL (UNII: 6UYK2W1W1E) (Active Moiety)
- SESAME OIL (UNII: QX10HYY4QV)
- SESAME OIL (UNII: QX10HYY4QV) (Active Moiety)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M)
- FUCUS VESICULOSUS (UNII: 535G2ABX9M) (Active Moiety)
- IODINE (UNII: 9679TC07X4)
- IODINE (UNII: 9679TC07X4) (Active Moiety)
- THYROID, PORCINE (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- BORAGE OIL (UNII: F8XAG1755S)
- BORAGE OIL (UNII: F8XAG1755S) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- CHLORIDE ION (UNII: Q32ZN48698) (Active Moiety)
- ANEMONE PRATENSIS (UNII: 8E272251DI)
- ANEMONE PRATENSIS (UNII: 8E272251DI) (Active Moiety)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Thyroid Tonic 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)
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[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".