NDC 67751-167 Tylenol Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
67751-167
Proprietary Name:
Tylenol Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Navajo Manufacturing Company Inc.
Labeler Code:
67751
Start Marketing Date: [9]
12-04-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OVAL (C48345)
Size(s):
19 MM
Imprint(s):
TYLENOL;500
Score:
1

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?

The NDC code 67751-167 is assigned by the FDA to the product Tylenol Extra Strength which is product labeled by Navajo Manufacturing Company Inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 67751-167-01 1 pouch in 1 carton / 2 tablet, film coated in 1 pouch, 67751-167-02 1 pouch in 1 carton / 4 tablet, film coated in 1 pouch, 67751-167-03 2 tray in 1 pouch / 12 tablet in 1 tray, 67751-167-04 12 pouch in 1 tray / 1 tablet, film coated in 1 pouch. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Tylenol Extra Strength?

Do not take more than directed (see overdose warning) adults and children 12 years and over• take 2 caplets every 6 hours while symptoms last• do not take more than 6 caplets in 24 hours, unless directed by a doctor• do not use for more than 10 days unless directed by a doctor children under 12 years ask a doctor

Which are Tylenol Extra Strength UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Tylenol Extra Strength?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[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".