NDC 55287-100 Green Tussin DM
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Product Details
What is NDC 55287-100?
Which are Green Tussin DM UNII Codes?
The UNII codes for the active ingredients in this product are:
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
Which are Green Tussin 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ALOE (UNII: V5VD430YW9)
- GINGER (UNII: C5529G5JPQ)
- CAT'S CLAW (UNII: 9060PRM18Q)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- PEPPERMINT (UNII: V95R5KMY2B)
- MENTHOL (UNII: L7T10EIP3A)
- ONION (UNII: 492225Q21H)
- GARLIC (UNII: V1V998DC17)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- CARAMEL (UNII: T9D99G2B1R)
- HONEY (UNII: Y9H1V576FH)
- CORN SYRUP (UNII: 9G5L16BK6N)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Green Tussin DM?
- RxCUI: 1298228 - dextromethorphan HBr 10 MG / guaiFENesin 100 MG in 15 mL Oral Solution
- RxCUI: 1298228 - dextromethorphan hydrobromide 0.667 MG/ML / guaifenesin 6.67 MG/ML Oral Solution
- RxCUI: 1298228 - dextromethorphan hydrobromide 10 MG / guaifenesin 100 MG per 15 ML Oral Solution
- RxCUI: 1298228 - dextromethorphan hydrobromide 20 MG / guaifenesin 200 MG per 30 ML Oral Solution
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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".