NDC 68016-242 Infants Pain Relief Oral Suspension Grape Flavor
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68016-242?
What are the uses for Infants Pain Relief Oral Suspension Grape Flavor?
Which are Infants Pain Relief Oral Suspension Grape Flavor UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Infants Pain Relief Oral Suspension Grape Flavor 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)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GLYCERIN (UNII: PDC6A3C0OX)
- HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITOL (UNII: 506T60A25R)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- XANTHAN GUM (UNII: TTV12P4NEE)
What is the NDC to RxNorm Crosswalk for Infants Pain Relief Oral Suspension Grape Flavor?
- RxCUI: 307668 - acetaminophen 160 MG in 5 mL Oral Suspension
- RxCUI: 307668 - acetaminophen 32 MG/ML Oral Suspension
- RxCUI: 307668 - acetaminophen 160 MG per 5 ML Oral Suspension
- RxCUI: 307668 - acetaminophen 320 MG per 10 ML Oral Suspension
- RxCUI: 307668 - acetaminophen 650 MG per 20.3 ML Oral Suspension
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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".