NDC 72689-0019 Geworin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72689 - Oasis Trading
- 72689-0019 - Geworin
Product Characteristics
Product Packages
NDC Code 72689-0019-1
Package Description: 10 TABLET in 1 BLISTER PACK
Product Details
What is NDC 72689-0019?
What are the uses for Geworin?
Which are Geworin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PROPYPHENAZONE (UNII: OED8FV75PY)
- PROPYPHENAZONE (UNII: OED8FV75PY) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
Which are Geworin 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:
- SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
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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".