NDC 63187-689 Cough And Cold
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 63187-689?
What are the uses for Cough And Cold?
Which are Cough And Cold UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
Which are Cough And Cold 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:
- ACACIA (UNII: 5C5403N26O)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONES (UNII: FZ989GH94E)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Cough And Cold?
- RxCUI: 1421985 - chlorpheniramine maleate 4 MG / dextromethorphan HBr 30 MG Oral Tablet
- RxCUI: 1421985 - chlorpheniramine maleate 4 MG / dextromethorphan hydrobromide 30 MG Oral Tablet
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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".