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  5. NDC Package Code: 55910-390-10 Menstrual Relief Maximum Strength

NDC Package 55910-390-10 Menstrual Relief Maximum Strength

Acetaminophen,Caffeine And Pyrilamine Maleate Tablet, Film Coated Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
55910-390-10
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Code:
55910-390
Proprietary Name:
Menstrual Relief Maximum Strength
Non-Proprietary Name:
Acetaminophen, Caffeine And Pyrilamine Maleate
Substance Name:
Acetaminophen; Caffeine; Pyrilamine Maleate
Usage Information:
Do not take more than the recommended doseadults and children 12 years and over: take 2 caplets with water repeat every 6 hours, as neededdo not exceed 6 caplets per daychildren under 12 years: ask a doctor
11-Digit NDC Billing Format:
55910039010
NDC to RxNorm Crosswalk:
  • RxCUI: 1597298 - acetaminophen 500 MG / caffeine 60 MG / pyrilamine maleate 15 MG Oral Tablet
  • RxCUI: 1597298 - APAP 500 MG / Caffeine 60 MG / Pyrilamine Maleate 15 MG Oral Tablet
Product Type:
Human Otc Drug
Labeler Name:
Dolgencorp, Llc
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):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M013
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
04-29-2002
End Marketing Date:
03-05-2026
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 55910-390-10?

The NDC Packaged Code 55910-390-10 is assigned to a package of 1 bottle, plastic in 1 carton / 40 tablet, film coated in 1 bottle, plastic of Menstrual Relief Maximum Strength, a human over the counter drug labeled by Dolgencorp, Llc. The product's dosage form is tablet, film coated and is administered via oral form.

Is NDC 55910-390 included in the NDC Directory?

Yes, Menstrual Relief Maximum Strength with product code 55910-390 is active and included in the NDC Directory. The product was first marketed by Dolgencorp, Llc on April 29, 2002.

What is the 11-digit format for NDC 55910-390-10?

The 11-digit format is 55910039010. 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
5-3-255910-390-105-4-255910-0390-10