NDC 67751-167 Tylenol Extra Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67751 - Navajo Manufacturing Company Inc.
- 67751-167 - Tylenol Extra Strength
Product Characteristics
Product Packages
NDC Code 67751-167-01
Package Description: 1 POUCH in 1 CARTON / 2 TABLET, FILM COATED in 1 POUCH
NDC Code 67751-167-02
Package Description: 1 POUCH in 1 CARTON / 4 TABLET, FILM COATED in 1 POUCH
NDC Code 67751-167-03
Package Description: 2 TRAY in 1 POUCH / 12 TABLET in 1 TRAY
NDC Code 67751-167-04
Package Description: 12 POUCH in 1 TRAY / 1 TABLET, FILM COATED in 1 POUCH
Product Details
What is NDC 67751-167?
What are the uses for Tylenol Extra Strength?
Which are Tylenol Extra Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
Which are Tylenol Extra Strength 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Tylenol Extra Strength?
- RxCUI: 198440 - acetaminophen 500 MG Oral Tablet
- RxCUI: 198440 - APAP 500 MG Oral Tablet
- RxCUI: 209459 - Tylenol Extra Strength 500 MG Oral Tablet
- RxCUI: 209459 - acetaminophen 500 MG Oral Tablet [Tylenol]
- RxCUI: 209459 - APAP 500 MG Oral Tablet [Tylenol]
* 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".