1. Home
  2. Labeler Index
  3. Mckesson Corp Via Strategic Sourcing Services Llc
  4. NDC Product Code: 62011-0484 Healthmart Earwax Removal Kit Ear Wax Drops And Bulb

NDC 62011-0484 Healthmart Earwax Removal Kit Ear Wax Drops And Bulb

Carbamide Peroxide Kit Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62011-0484?
  4. Healthmart Earwax Removal Kit Ear Wax Drops And Bulb Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
62011-0484
Proprietary Name:
Healthmart Earwax Removal Kit Ear Wax Drops And Bulb
Non-Proprietary Name: [1]
Carbamide Peroxide
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.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Labeler Name: [5]
    Mckesson Corp Via Strategic Sourcing Services Llc
    Labeler Code:
    62011
    Product Label ID:
    4229f02a-bd71-4d27-94d6-ae860bd60d20
    FDA Application Number: [6]
    M014
    Marketing Category: [8]
    OTC MONOGRAPH DRUG -
    Start Marketing Date: [9]
    02-25-2022
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 62011-0484?

    The NDC code 62011-0484 is assigned by the FDA to the product Healthmart Earwax Removal Kit Ear Wax Drops And Bulb which is a human over the counter drug product labeled by Mckesson Corp Via Strategic Sourcing Services Llc. The generic name of Healthmart Earwax Removal Kit Ear Wax Drops And Bulb is carbamide peroxide. The product's dosage form is kit and is administered via topical form. The product is distributed in a single package with assigned NDC code 62011-0484-1 1 kit in 1 kit * 1 bottle in 1 box (62011-0483-1) / 15 ml in 1 bottle. 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 Healthmart Earwax Removal Kit Ear Wax Drops And Bulb?

    This medication is used to treat earwax buildup. It helps to soften, loosen, and remove the earwax. Too much earwax can block the ear canal and reduce hearing. This medication releases oxygen and starts to foam when it comes in contact with the skin. The foaming helps break up and remove the earwax. Consult your doctor before using this product in children younger than 12 years.

    Which are Healthmart Earwax Removal Kit Ear Wax Drops And Bulb UNII Codes?

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

    Which are Healthmart Earwax Removal Kit Ear Wax Drops And Bulb 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 Healthmart Earwax Removal Kit Ear Wax Drops And Bulb?

    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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [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".