NDC 13411-841 Acetaflu Nighttime Effervescent
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13411 - Advanced Pharmaceutical Services, Inc. Dba Affordable Quality Pharmaceuticals
- 13411-841 - Acetaflu Nighttime Effervescent
Product Characteristics
Product Packages
NDC Code 13411-841-16
Package Description: 4 BLISTER PACK in 1 BOX / 4 TABLET, EFFERVESCENT in 1 BLISTER PACK
Product Details
What is NDC 13411-841?
Which are Acetaflu Nighttime Effervescent UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
- DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)
- PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ)
- PHENYLEPHRINE (UNII: 1WS297W6MV) (Active Moiety)
Which are Acetaflu Nighttime Effervescent 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:
- MANNITOL (UNII: 3OWL53L36A)
- ASPARTAME (UNII: Z0H242BBR1)
- POVIDONE K30 (UNII: U725QWY32X)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- DIMETHICONE (UNII: 92RU3N3Y1O)
What is the NDC to RxNorm Crosswalk for Acetaflu Nighttime Effervescent?
- RxCUI: 2287739 - acetaminophen 650 MG / diphenhydrAMINE HCl 25 MG / phenylephrine HCl 10 MG Effervescent Oral Tablet
- RxCUI: 2287739 - acetaminophen 650 MG / diphenhydramine hydrochloride 25 MG / phenylephrine hydrochloride 10 MG Effervescent Oral Tablet
- RxCUI: 2287739 - acetaminophen 650 MG / diphenhydramine HCl 25 MG / phenylephrine HCl 10 MG Effervescent Oral Tablet
- RxCUI: 2287739 - APAP 650 MG / Diphenhydramine Hydrochloride 25 MG / Phenylephrine Hydrochloride 10 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".