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  5. NDC Package Code: 0573-2919-12 Preparation H

NDC Package 0573-2919-12 Preparation H

Phenylephrine Hydrochloride Suppository Rectal - 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:
0573-2919-12
Package Description:
12 BLISTER PACK in 1 CARTON / 1 SUPPOSITORY in 1 BLISTER PACK
Product Code:
0573-2919
Proprietary Name:
Preparation H
Non-Proprietary Name:
Phenylephrine Hydrochloride
Substance Name:
Phenylephrine Hydrochloride
Usage Information:
Adults: when practical, cleanse the affected area by patting or blotting with an appropriate cleansing wipe. Gently dry by patting or blotting with a tissue or a soft cloth before insertion of this product.detach one suppository from the strip; remove the foil wrapper before inserting into the rectum as follows: hold suppository with the rounded end upas shown, carefully separate foil tabs by inserting tip of fingernail at end marked “peel down”slowly and evenly peel apart (do not tear) foil by pulling tabs down both sides, to expose the suppositoryremove exposed suppository from the wrapperinsert one suppository into the rectum up to 4 times daily, especially at night, in the morning or after each bowel movementchildren under 12 years of age: consult a doctor
11-Digit NDC Billing Format:
00573291912
Product Type:
Human Otc Drug
Labeler Name:
Haleon Us Holdings Llc
Dosage Form:
Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
Administration Route(s):
Rectal - Administration to the rectum.
Active Ingredient(s):
PHENYLEPHRINE HYDROCHLORIDE 6.25 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
M015
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
04-30-2025
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0573-2919-12?

The NDC Packaged Code 0573-2919-12 is assigned to a package of 12 blister pack in 1 carton / 1 suppository in 1 blister pack of Preparation H, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is suppository and is administered via rectal form.

Is NDC 0573-2919 included in the NDC Directory?

Yes, Preparation H with product code 0573-2919 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on April 30, 2025 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 0573-2919-12?

The 11-digit format is 00573291912. 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 4-4-2 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
4-4-20573-2919-125-4-200573-2919-12