NDC 13411-854 Acetamax
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 13411-854-16
Package Description: 16 BLISTER PACK in 1 BOX / 1 TABLET, EFFERVESCENT in 1 BLISTER PACK
NDC Code 13411-854-20
Package Description: 20 BLISTER PACK in 1 BOX / 1 TABLET, EFFERVESCENT in 1 BLISTER PACK
NDC Code 13411-854-24
Package Description: 24 BLISTER PACK in 1 BOX / 1 TABLET, EFFERVESCENT in 1 BLISTER PACK
Product Details
What is NDC 13411-854?
What are the uses for Acetamax?
Which are Acetamax UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Acetamax 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- GINGER OIL (UNII: SAS9Z1SVUK)
- WEST INDIAN LEMONGRASS OIL (UNII: 5BIA40E9ED)
- MANNITOL (UNII: 3OWL53L36A)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- POVIDONE K30 (UNII: U725QWY32X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Acetamax?
- RxCUI: 1536880 - acetaminophen 500 MG Effervescent Oral Tablet
- RxCUI: 1536880 - APAP 500 MG Effervescent Oral Tablet
* Please review the disclaimer below.
[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".