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  5. NDC Package Code: 52301-303-25 Formula 303

NDC Package 52301-303-25 Formula 303

Valerian Root,Passiflora,Magnesium Carbonate Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
52301-303-25
Package Description:
250 TABLET in 1 BOTTLE
Product Code:
52301-303
Proprietary Name:
Formula 303
Non-Proprietary Name:
Valerian Root, Passiflora, Magnesium Carbonate
Substance Name:
Magnesium Carbonate; Passiflora Incarnata Flower; Valerian
Usage Information:
MUSCLE SPASM: As a muscle relaxant, two tablets every three hours until relief is obtained. Then two tablets with each meal and two and bedtime.TENSION AND STRESS: As a relaxant, two tablets with each meal and two at bedtime.
11-Digit NDC Billing Format:
52301030325
Product Type:
Human Otc Drug
Labeler Name:
Dee Cee Laboratories
Dosage Form:
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • MAGNESIUM CARBONATE 1 [hp_X]/1
  • PASSIFLORA INCARNATA FLOWER 3 [hp_X]/1
  • VALERIAN 6 [hp_X]/1
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-19-1990
    Listing Expiration Date:
    12-31-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    52301-303-12120 TABLET in 1 BOTTLE
    52301-303-2112 TABLET in 1 BAG
    52301-303-30300 TABLET in 1 BOTTLE
    52301-303-4545 TABLET in 1 BOTTLE
    52301-303-6060 TABLET in 1 BOTTLE
    52301-303-9090 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 52301-303-25?

    The NDC Packaged Code 52301-303-25 is assigned to a package of 250 tablet in 1 bottle of Formula 303, a human over the counter drug labeled by Dee Cee Laboratories. The product's dosage form is tablet and is administered via oral form.

    Is NDC 52301-303 included in the NDC Directory?

    Yes, Formula 303 with product code 52301-303 is active and included in the NDC Directory. The product was first marketed by Dee Cee Laboratories on September 19, 1990 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 52301-303-25?

    The 11-digit format is 52301030325. 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
    5-3-252301-303-255-4-252301-0303-25