NDC 57955-5053 Lungs And Bronchial Relief
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 57955-5053?
What are the uses for Lungs And Bronchial Relief?
Which are Lungs And Bronchial Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMMONIUM CARBONATE (UNII: NJ5VT0FKLJ)
- AMMONIUM CATION (UNII: 54S68520I4) (Active Moiety)
- ANTIMONY ARSENATE (UNII: WE3458XNFT)
- ANTIMONY ARSENATE (UNII: WE3458XNFT) (Active Moiety)
- ANTIMONY POTASSIUM TARTRATE (UNII: DL6OZ476V3)
- ANTIMONY (UNII: 9IT35J3UV3) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO) (Active Moiety)
- BROMINE (UNII: SBV4XY874G)
- BROMINE (UNII: SBV4XY874G) (Active Moiety)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- CHLORINE (UNII: 4R7X1O2820)
- CHLORINE (UNII: 4R7X1O2820) (Active Moiety)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- TIN (UNII: 387GMG9FH5)
- TIN (UNII: 387GMG9FH5) (Active Moiety)
- SULFURIC ACID (UNII: O40UQP6WCF)
- SULFURIC ACID (UNII: O40UQP6WCF) (Active Moiety)
Which are Lungs And Bronchial Relief 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)
* 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".