NDC 21695-517 Delsym
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 21695-517?
What are the uses for Delsym?
Which are Delsym UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROMETHORPHAN (UNII: 7355X3ROTS)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
Which are Delsym 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SUCROSE (UNII: C151H8M554)
- TRAGACANTH (UNII: 2944357O2O)
- CORN OIL (UNII: 8470G57WFM)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Delsym?
- RxCUI: 1373045 - dextromethorphan polistirex 30 MG in 5 mL 12HR Extended Release Oral Suspension
- RxCUI: 1373045 - 12 HR dextromethorphan polistirex 6 MG/ML Extended Release Suspension
- RxCUI: 1373045 - dextromethorphan polistirex (dextromethorphan HBr 30 MG) per 5 ML 12 HR Extended Release Suspension
- RxCUI: 1373045 - dextromethorphan polistirex 6 MG/ML 12 HR Extended Release Suspension
- RxCUI: 1373128 - Delsym 30 MG in 5 mL 12HR Extended Release Oral Suspension
* 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".