NDC 67510-0523 Day Time Gelcap
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67510 - Kareway Product, Inc.
- 67510-0523 - Day Time Gelcap
Product Characteristics
Product Packages
NDC Code 67510-0523-0
Package Description: 2 BLISTER PACK in 1 BOX / 20 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
NDC Code 67510-0523-1
Package Description: 1 BLISTER PACK in 1 BOX / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
NDC Code 67510-0523-2
Package Description: 1 BLISTER PACK in 1 BOX / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
NDC Code 67510-0523-4
Package Description: 2 BLISTER PACK in 1 BOX / 24 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Details
What is NDC 67510-0523?
What are the uses for Day Time Gelcap?
Which are Day Time Gelcap UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Day Time Gelcap 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:
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL, (R)- (UNII: 602HN5L69H)
- WATER (UNII: 059QF0KO0R)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Day Time Gelcap?
- RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
- RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
- RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
* 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".