NDC 23359-033 Ninjacof-a
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 23359-033?
What are the uses for Ninjacof-a?
Which are Ninjacof-a UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y)
- CHLOPHEDIANOL (UNII: 42C50P12AP) (Active Moiety)
- PYRILAMINE MALEATE (UNII: R35D29L3ZA)
- PYRILAMINE (UNII: HPE317O9TL) (Active Moiety)
Which are Ninjacof-a 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
What is the NDC to RxNorm Crosswalk for Ninjacof-a?
- RxCUI: 1593765 - acetaminophen 160 MG / chlophedianol HCl 12.5 MG / pyrilamine maleate 12.5 MG in 5 mL Oral Solution
- RxCUI: 1593765 - acetaminophen 32 MG/ML / chlophedianol hydrochloride 2.5 MG/ML / pyrilamine maleate 2.5 MG/ML Oral Solution
- RxCUI: 1593765 - acetaminophen 160 MG / chlophedianol hydrochloride 12.5 MG / pyrilamine maleate 12.5 MG per 5 ML Oral Solution
- RxCUI: 1593765 - APAP 32 MG/ML / chlophedianol hydrochloride 2.5 MG/ML / Pyrilamine Maleate 2.5 MG/ML Oral Solution
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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".