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  5. NDC Package Code: 0573-2868-98 Preparation H Maximum Strength

NDC Package 0573-2868-98 Preparation H Maximum Strength

Glycerin,Petrolatum,Phenylephrine Hcl,Pramoxine Hcl Cream Topical - 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:
0573-2868-98
Package Description:
1 TUBE in 1 CARTON / 51 g in 1 TUBE
Product Code:
0573-2868
Proprietary Name:
Preparation H Maximum Strength
Non-Proprietary Name:
Glycerin, Petrolatum, Phenylephrine Hcl, Pramoxine Hcl
Substance Name:
Glycerin; Petrolatum; Phenylephrine Hydrochloride; Pramoxine 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 applying cream.when first opening the tube, puncture foil seal with top end of capapply externally or in the lower portion of the anal canal onlyapply externally to the affected area up to 4 times daily, especially at night, in the morning or after each bowel movementfor application in the lower anal canal: remove cover from dispensing cap. Attach dispensing cap to tube. Lubricate dispensing cap well, then gently insert dispensing cap partway into the anus.thoroughly cleanse dispensing cap after each use and replace coverchildren under 12 years of age: ask a doctor
11-Digit NDC Billing Format:
00573286898
NDC to RxNorm Crosswalk:
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine HCl 0.25 % / pramoxine HCl 1 % / white petrolatum 15 % Rectal Cream
  • RxCUI: 1293649 - glycerin 144 MG/ML / petrolatum 150 MG/ML / phenylephrine hydrochloride 2.5 MG/ML / pramoxine hydrochloride 10 MG/ML Rectal Cream
  • RxCUI: 1293649 - glycerin 14.4 % / phenylephrine hydrochloride 0.25 % / pramoxine hydrochloride 1 % / white petrolatum 15 % Rectal Cream
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Haleon Us Holdings Llc
    Dosage Form:
    Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • GLYCERIN 144 mg/g
  • PETROLATUM 150 mg/g
  • PHENYLEPHRINE HYDROCHLORIDE 2.5 mg/g
  • PRAMOXINE HYDROCHLORIDE 10 mg/g
    • Pharmacologic Class(es):
  • Adrenergic alpha1-Agonists - [MoA] (Mechanism of Action)
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Glycerol - [CS]
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Increased IgG Production - [PE] (Physiologic Effect)
  • Non-Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • alpha-1 Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M015
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-01-2004
    Listing Expiration Date:
    12-31-2025
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0573-2868-101 TUBE in 1 CARTON / 26 g in 1 TUBE
    0573-2868-201 TUBE in 1 CARTON / 51 g in 1 TUBE
    0573-2868-931 TUBE in 1 CARTON / 26 g in 1 TUBE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0573-2868-98?

    The NDC Packaged Code 0573-2868-98 is assigned to a package of 1 tube in 1 carton / 51 g in 1 tube of Preparation H Maximum Strength, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is cream and is administered via topical form.

    Is NDC 0573-2868 included in the NDC Directory?

    Yes, Preparation H Maximum Strength with product code 0573-2868 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on July 01, 2004 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0573-2868-98?

    The 11-digit format is 00573286898. 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
    4-4-20573-2868-985-4-200573-2868-98