NDC 68016-026 Adult Long Lasting-cough Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68016 - Chain Drug Consortium Llc
- 68016-026 - Adult Long Lasting-cough Relief
Product Characteristics
Product Packages
NDC Code 68016-026-20
Package Description: 1 BOTTLE in 1 CARTON / 20 CAPSULE in 1 BOTTLE
Product Details
What is NDC 68016-026?
What are the uses for Adult Long Lasting-cough Relief?
Which are Adult Long Lasting-cough Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
Which are Adult Long Lasting-cough 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:
- GELATIN (UNII: 2G86QN327L)
- SORBITAN (UNII: 6O92ICV9RU)
- SORBITOL (UNII: 506T60A25R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- WATER (UNII: 059QF0KO0R)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POVIDONE K30 (UNII: U725QWY32X)
- GLYCERIN (UNII: PDC6A3C0OX)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Adult Long Lasting-cough Relief?
- RxCUI: 1090487 - dextromethorphan HBr 15 MG Oral Capsule
- RxCUI: 1090487 - dextromethorphan hydrobromide 15 MG Oral Capsule
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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".