NDC 57520-0363 Tinnitus DX
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57520 - Apotheca Company
- 57520-0363 - Tinnitus
Product Characteristics
Product Packages
NDC Code 57520-0363-1
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 57520-0363?
What are the uses for Tinnitus DX?
Which are Tinnitus DX 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)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- QUININE SULFATE (UNII: KF7Z0E0Q2B)
- QUININE (UNII: A7V27PHC7A) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB)
- CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (Active Moiety)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72) (Active Moiety)
- GRAPHITE (UNII: 4QQN74LH4O)
- GRAPHITE (UNII: 4QQN74LH4O) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479)
- LYCOPODIUM CLAVATUM SPORE (UNII: C88X29Y479) (Active Moiety)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SODIUM CATION (UNII: LYR4M0NH37) (Active Moiety)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Tinnitus DX 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- THIAMINE MONONITRATE (UNII: 8K0I04919X)
- NIACIN (UNII: 2679MF687A)
- INOSITOL NIACINATE (UNII: A99MK953KZ)
- FOLIC ACID (UNII: 935E97BOY8)
- METHYLCOBALAMIN (UNII: BR1SN1JS2W)
- MAGNESIUM CITRATE (UNII: RHO26O1T9V)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- SELENIUM (UNII: H6241UJ22B)
- COPPER GLUCONATE (UNII: RV823G6G67)
- MANGANESE (UNII: 42Z2K6ZL8P)
- ACETYLCYSTEINE (UNII: WYQ7N0BPYC)
- IPRIFLAVONE (UNII: 80BJ7WN25Z)
- GINKGO (UNII: 19FUJ2C58T)
- GINGER (UNII: C5529G5JPQ)
- ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)
- GARLIC (UNII: V1V998DC17)
- AMINOBENZOIC ACID (UNII: TL2TJE8QTX)
- BLACK COHOSH (UNII: K73E24S6X9)
- VINPOCETINE (UNII: 543512OBTC)
- BLACK PEPPER (UNII: KM66971LVF)
- UBIDECARENONE (UNII: EJ27X76M46)
- GELATIN (UNII: 2G86QN327L)
- RICE (UNII: 659G217HPG)
- CHROMIUM (UNII: 0R0008Q3JB)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
* 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".