NDC 53113-217 Broncomar DM
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What is NDC 53113-217?
What are the uses for Broncomar DM?
Which are Broncomar DM UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
Which are Broncomar DM 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:
- CAULOPHYLLUM THALICTROIDES ROOT (UNII: JTJ6HH6YEH)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- ECHINACEA, UNSPECIFIED (UNII: 4N9P6CC1DX)
- EUCALYPTUS CAMALDULENSIS LEAF OIL (UNII: SN6D1J15I6)
- GINKGO BILOBA WHOLE (UNII: 660486U6OI)
- GOLDENSEAL (UNII: ZW3Z11D0JV)
- HONEY (UNII: Y9H1V576FH)
- HOREHOUND (UNII: K08036XEJV)
- LICORICE (UNII: 61ZBX54883)
- MENTHOL (UNII: L7T10EIP3A)
- MULLEIN LEAF (UNII: 9936O846LI)
- MYRRH (UNII: JC71GJ1F3L)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ULMUS RUBRA BARK (UNII: 91QY4PXU8Q)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
- ZINC SULFATE (UNII: 89DS0H96TB)
What is the NDC to RxNorm Crosswalk for Broncomar DM?
- RxCUI: 996520 - dextromethorphan HBr 20 MG / guaiFENesin 200 MG in 10 mL Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 2 MG/ML / guaifenesin 20 MG/ML Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 5 ML Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 15 MG / guaifenesin 150 MG per 7.5 ML Oral Solution
- RxCUI: 996520 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 10 ML Oral Solution
* 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".