NDC 72689-0013 Facol Classic One
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72689 - Oasis Trading
- 72689-0013 - Facol Classic One
Product Characteristics
Product Packages
NDC Code 72689-0013-1
Package Description: 10 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 72689-0013?
What are the uses for Facol Classic One?
Which are Facol Classic One UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- GUAIFENESIN (UNII: 495W7451VQ)
- GUAIFENESIN (UNII: 495W7451VQ) (Active Moiety)
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
- METHYLEPHEDRINE HYDROCHLORIDE, (+/-)- (UNII: 99214P83XM)
- METHYLEPHEDRINE, (+/-)- (UNII: SHS9PGQ2LS) (Active Moiety)
- CLOPERASTINE HYDROCHLORIDE (UNII: PI4N7C63ND)
- CLOPERASTINE (UNII: 69M5L7BXEK) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
Which are Facol Classic One 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:
- STARCH, CORN (UNII: O8232NY3SJ)
* 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".