NDC 76168-021 Pain Reliever Fever Reducer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76168 - Velocity Pharma
- 76168-021 - Pain Reliever Fever Reducer
Product Characteristics
Product Packages
NDC Code 76168-021-13
Package Description: 6 CARTON in 1 BLISTER PACK / 1 TABLET, EFFERVESCENT in 1 CARTON
Product Details
What is NDC 76168-021?
What are the uses for Pain Reliever Fever Reducer?
Which are Pain Reliever Fever Reducer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH)
- DEXTROMETHORPHAN (UNII: 7355X3ROTS) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
- CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)
- CHLORPHENIRAMINE (UNII: 3U6IO1965U) (Active Moiety)
Which are Pain Reliever Fever Reducer 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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- ASPARTAME (UNII: Z0H242BBR1)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- PONCEAU 4R (UNII: Z525CBK9PG)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- MANNITOL (UNII: 3OWL53L36A)
- ORANGE (UNII: 5EVU04N5QU)
- POVIDONE K30 (UNII: U725QWY32X)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
What is the NDC to RxNorm Crosswalk for Pain Reliever Fever Reducer?
- RxCUI: 1536477 - acetaminophen 250 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Effervescent Oral Tablet
- RxCUI: 1536477 - acetaminophen 250 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Effervescent Oral Tablet
- RxCUI: 1536477 - APAP 250 MG / Chlorpheniramine Maleate 2 MG / Dextromethorphan Hydrobromide 10 MG / Phenylephrine Hydrochloride 5 MG Effervescent Oral Tablet
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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".