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  4. NDC Product Code: 0573-2884 Preparation H

NDC 0573-2884 Preparation H

Cocoa Butter,Phenylephrine Hydrochloride,And Witch Hazel Kit - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0573-2884?
  5. Preparation H Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
0573-2884
Proprietary Name:
Preparation H
Non-Proprietary Name: [1]
Cocoa Butter, Phenylephrine Hydrochloride, And Witch Hazel
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Haleon Us Holdings Llc
Labeler Code:
0573
Product Label ID:
2f370875-0225-47b7-b43f-8fa4600d2a0e
FDA Application Number: [6]
M015
Marketing Category: [8]
OTC MONOGRAPH DRUG -
Start Marketing Date: [9]
07-01-2015
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330 - LIGHT YELLOW)
WHITE (C48325 - WHITE)

Code Structure Chart

Product Details

What is NDC 0573-2884?

The NDC code 0573-2884 is assigned by the FDA to the product Preparation H which is a human over the counter drug product labeled by Haleon Us Holdings Llc. The generic name of Preparation H is cocoa butter, phenylephrine hydrochloride, and witch hazel. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 0573-2884-12 1 kit in 1 carton * 12 suppository in 1 blister pack * 4 cloth in 1 applicator. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Preparation H?

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 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 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: ask a doctor adults: unfold wipe and cleanse the area by gently wiping, patting or blotting. If necessary, repeat until all matter is removed from the area.use up to 6 times daily or after each bowel movement and before applying topical hemorrhoidal treatments, and then discardchildren under 12 years of age: consult a doctor

Which are Preparation H UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Preparation H Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Preparation H?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".