NDC 49035-026 Acetaminophen And Diphenhydramine Hydrochloride

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:
49035-026
Proprietary Name:
Acetaminophen And Diphenhydramine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walmart Stores Inc
Labeler Code:
49035
Start Marketing Date: [9]
06-01-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
OVAL (C48345)
Size(s):
18 MM
Imprint(s):
S525
Score:
1

Product Packages

NDC Code 49035-026-20

Package Description: 2 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE

NDC Code 49035-026-50

Package Description: 1 BOTTLE in 1 CARTON / 50 TABLET, FILM COATED in 1 BOTTLE

Product Details

What is NDC 49035-026?

The NDC code 49035-026 is assigned by the FDA to the product Acetaminophen And Diphenhydramine Hydrochloride which is product labeled by Walmart Stores Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 49035-026-20 2 bottle in 1 carton / 100 tablet, film coated in 1 bottle, 49035-026-50 1 bottle in 1 carton / 50 tablet, film coated in 1 bottle. 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 Acetaminophen And Diphenhydramine Hydrochloride?

Do not take more than recommended (see overdose warning)adults and children 12 years of age and over:take 2 caplets at bedtime or as directed by a doctordo not take more than 2 caplets in a 24 hour periodchildren under 12 years of age:do not use this adult product in children under 12 years of age. This will provide more than the recommended dose (overdose) and may cause liver damage

Which are Acetaminophen And Diphenhydramine Hydrochloride UNII Codes?

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

Which are Acetaminophen And Diphenhydramine Hydrochloride 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 Acetaminophen And Diphenhydramine Hydrochloride?

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:
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydrAMINE HCl 25 MG Oral Tablet
  • RxCUI: 1092189 - acetaminophen 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet
  • RxCUI: 1092189 - APAP 500 MG / diphenhydramine hydrochloride 25 MG Oral Tablet

* 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".