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  5. NDC Package Code: 29485-6931-6 Benadryl

NDC Package 29485-6931-6 Benadryl

Diphenhydramine Hydrochloride Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
29485-6931-6
Package Description:
3 POUCH in 1 BLISTER PACK / 2 TABLET, FILM COATED in 1 POUCH
Product Code:
29485-6931
Proprietary Name:
Benadryl
Non-Proprietary Name:
Diphenhydramine Hydrochloride
Substance Name:
Diphenhydramine Hydrochloride
Usage Information:
Take every 4 to 6 hours, or as directed by a doctordo not take more than 6 times in 24 hoursadults and children 12 years and over1 to 2 tabletschildren 6 to under 12 years1 tabletchildren under 6 yearsdo not use
11-Digit NDC Billing Format:
29485693106
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Lil' Drug Store Products, Inc.
Dosage Form:
Tablet, Film Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is coated with a thin layer of a water-insoluble or water-soluble polymer.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
DIPHENHYDRAMINE HYDROCHLORIDE 25 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
02-06-2017
End Marketing Date:
11-07-2025
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 29485-6931-6?

The NDC Packaged Code 29485-6931-6 is assigned to a package of 3 pouch in 1 blister pack / 2 tablet, film coated in 1 pouch of Benadryl, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 29485-6931 included in the NDC Directory?

Yes, Benadryl with product code 29485-6931 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on February 06, 2017.

What is the 11-digit format for NDC 29485-6931-6?

The 11-digit format is 29485693106. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-4-129485-6931-65-4-229485-6931-06