NDC Package 59779-894-12 Pain Relief Pm

Acetaminophen,Aspirin,Diphenhydramine Citrate Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

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:
59779-894-12
Package Description:
1 BOTTLE in 1 CARTON / 100 TABLET, FILM COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Pain Relief Pm
Non-Proprietary Name:
Acetaminophen, Aspirin, Diphenhydramine Citrate
Substance Name:
Acetaminophen; Aspirin; Diphenhydramine Citrate
Usage Information:
Do not take more than directedadults and children 12 years and over: take 2 caplets at bedtime, with a full glass of waterdo not take more than 2 caplets in 24 hours, unless directed by a doctorchildren under 12 years: do not use
11-Digit NDC Billing Format:
59779089412
NDC to RxNorm Crosswalk:
  • RxCUI: 1593110 - acetaminophen 250 MG / aspirin 250 MG / diphenhydrAMINE citrate 38 MG Oral Tablet
  • RxCUI: 1593110 - acetaminophen 250 MG / aspirin 250 MG / diphenhydramine citrate 38 MG Oral Tablet
  • RxCUI: 1593110 - APAP 250 MG / ASA 250 MG / Diphenhydramine Citrate 38 MG Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Cvs Pharmacy
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.
Sample Package:
No
FDA Application Number:
M013
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-31-2016
Listing Expiration Date:
12-31-2026
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.

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Frequently Asked Questions

What is NDC 59779-894-12?

The NDC Packaged Code 59779-894-12 is assigned to a package of 1 bottle in 1 carton / 100 tablet, film coated in 1 bottle of Pain Relief Pm, a human over the counter drug labeled by Cvs Pharmacy. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 59779-894 included in the NDC Directory?

Yes, Pain Relief Pm with product code 59779-894 is active and included in the NDC Directory. The product was first marketed by Cvs Pharmacy on August 31, 2016 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 59779-894-12?

The 11-digit format is 59779089412. 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 5-3-2 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
5-3-259779-894-125-4-259779-0894-12