NDC 17856-1986 Childrens Mapap Acetaminophen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17856-1986?
What are the uses for Childrens Mapap Acetaminophen?
Which are Childrens Mapap Acetaminophen UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Childrens Mapap Acetaminophen 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITOL (UNII: 506T60A25R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PRUNUS SEROTINA BARK (UNII: 5D48E975HA)
- POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
What is the NDC to RxNorm Crosswalk for Childrens Mapap Acetaminophen?
- RxCUI: 209397 - Mapap Childrens 160 MG in 5 mL Oral Solution
- RxCUI: 209397 - acetaminophen 32 MG/ML Oral Solution [Mapap]
- RxCUI: 209397 - APAP 32 MG/ML Oral Solution [Mapap]
- RxCUI: 209397 - Mapap 160 mg per 5 mL Oral Solution
- RxCUI: 209397 - Mapap 32 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".