NDC 57955-5275 Ear Ringing
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57955-5275?
What are the uses for Ear Ringing?
Which are Ear Ringing UNII Codes?
The UNII codes for the active ingredients in this product are:
- ARNICA MONTANA (UNII: O80TY208ZW)
- ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- DYSPHANIA AMBROSIOIDES (UNII: 4H5RSU087I)
- CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (Active Moiety)
- QUININE SALICYLATE (UNII: 6DY04L71DR)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- BLACK COHOSH (UNII: K73E24S6X9)
- BLACK COHOSH (UNII: K73E24S6X9) (Active Moiety)
- COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E)
- COFFEA ARABICA SEED, ROASTED (UNII: 9H58JRT35E) (Active Moiety)
- POTASSIUM IODIDE (UNII: 1C4QK22F9J)
- IODIDE ION (UNII: 09G4I6V86Q) (Active Moiety)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18)
- KALMIA LATIFOLIA LEAF (UNII: 79N6542N18) (Active Moiety)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (Active Moiety)
- MANGANESE ACETATE TETRAHYDRATE (UNII: 9TO51D176N)
- MANGANESE CATION (2+) (UNII: H6EP7W5457) (Active Moiety)
- MANGANESE CARBONATE (UNII: 9ZV57512ZM)
- MERCURY (UNII: FXS1BY2PGL)
- MERCURY (UNII: FXS1BY2PGL) (Active Moiety)
- SODIUM SALICYLATE (UNII: WIQ1H85SYP)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- ALLYLTHIOUREA (UNII: 706IDJ14B7)
- ALLYLTHIOUREA (UNII: 706IDJ14B7) (Active Moiety)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P)
- THYROID, UNSPECIFIED (UNII: 0B4FDL9I6P) (Active Moiety)
Which are Ear Ringing 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)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".