NDC 63868-566 Qaulity Choice Pain Relief Regular Strength
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 63868-566?
What are the uses for Qaulity Choice Pain Relief Regular Strength?
Which are Qaulity Choice Pain Relief Regular Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Qaulity Choice Pain Relief Regular Strength 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:
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- 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 Qaulity Choice Pain Relief Regular Strength?
- RxCUI: 307675 - acetaminophen 160 MG in 5 mL Oral Solution
- RxCUI: 307675 - acetaminophen 32 MG/ML Oral Solution
- RxCUI: 307675 - acetaminophen 160 MG per 5 ML Oral Solution
- RxCUI: 307675 - acetaminophen 325 MG per 10.15 ML Oral Solution
- RxCUI: 307675 - acetaminophen 650 MG per 20.3 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".