NDC 46084-101 Acetaminophen Sinus Congestion And Pain A P J Coated
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 46084-101?
What are the uses for Acetaminophen Sinus Congestion And Pain A P J Coated?
Which are Acetaminophen Sinus Congestion And Pain A P J Coated UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Acetaminophen Sinus Congestion And Pain A P J Coated 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:
- CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- METHYLENE CHLORIDE (UNII: 588X2YUY0A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Acetaminophen Sinus Congestion And Pain A P J Coated?
- RxCUI: 1046378 - acetaminophen 325 MG / phenylephrine HCl 5 MG Oral Tablet
- RxCUI: 1046378 - acetaminophen 325 MG / phenylephrine hydrochloride 5 MG Oral Tablet
- RxCUI: 1046378 - APAP 325 MG / phenylephrine hydrochloride 5 MG 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".