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  4. NDC Product Code: 83872-017 Hydraheal Foot Cream

NDC 83872-017 Hydraheal Foot Cream

Glycerin And Vitamin E Foot Cream Liniment Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 83872-017?
  4. Hydraheal Foot Cream Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
83872-017
Proprietary Name:
Hydraheal Foot Cream
Non-Proprietary Name: [1]
Glycerin And Vitamin E Foot Cream
Substance Name: [2]
1,3-bis(benzothiazol-2-ylthiomethyl)urea; Honey; Tea Tree Oil
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liniment - A solution or mixture of various substances in oil, alcoholic solutions of soap, or emulsions intended for external application.
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]
    Shenzhen Xiaomai Manufacturing Co., Ltd.
    Labeler Code:
    83872
    Product Label ID:
    10c22a55-fe8f-608c-e063-6294a90a1ceb
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    02-07-2024
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 83872-017?

    The NDC code 83872-017 is assigned by the FDA to the product Hydraheal Foot Cream which is a human over the counter drug product labeled by Shenzhen Xiaomai Manufacturing Co., Ltd.. The generic name of Hydraheal Foot Cream is glycerin and vitamin e foot cream. The product's dosage form is liniment and is administered via topical form. The product is distributed in a single package with assigned NDC code 83872-017-01 50 ml in 1 bottle, pump . 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 Hydraheal Foot Cream?

    Apply the foot cream evenly onto clean feet, gently massage with fingertips, paying special attention to dry or rough areas. It is recommended for daily use, especially before bedtime, to maintain soft and moisturized foot skin and alleviate dryness, roughness, and foot fatigue.

    What are Hydraheal Foot Cream Active Ingredients?

    An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
    • 1,3-BIS(BENZOTHIAZOL-2-YLTHIOMETHYL)UREA 10 g/100mL
    • HONEY 3 g/100mL - A sweet viscous liquid food, produced in the honey sacs of various bees from nectar collected from flowers. The nectar is ripened into honey by inversion of its sucrose sugar into fructose and glucose. It is somewhat acidic and has mild antiseptic properties, being sometimes used in the treatment of burns and lacerations.
    • TEA TREE OIL 5 g/100mL - Essential oil extracted from MELALEUCA ALTERNIFOLIA (tea tree). It is used as a topical antimicrobial due to the presence of terpineol.

    Which are Hydraheal Foot Cream UNII Codes?

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

    Which are Hydraheal Foot Cream 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:

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    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.

    [2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

    [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.

    [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".