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  4. NDC Product Code: 62003-422 Tiger Balm Arthritis Rub

NDC 62003-422 Tiger Balm Arthritis Rub

Camphor (synthetic) And Menthol Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 62003-422?
  4. Tiger Balm Arthritis Rub Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

NDC Product Code:
62003-422
Proprietary Name:
Tiger Balm Arthritis Rub
Non-Proprietary Name: [1]
Camphor (synthetic) And Menthol
Substance Name: [2]
Camphor (synthetic); Menthol, Unspecified Form
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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): [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]
    Prince Of Peace Enterprises, Inc.
    Labeler Code:
    62003
    Product Label ID:
    11a18b43-0017-4159-8d4b-af58073e0d4e
    FDA Application Number: [6]
    part348
    Marketing Category: [8]
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date: [9]
    06-10-2002
    End Marketing Date: [10]
    02-28-2026
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 62003-422-02

    Package Description: 2 mL in 1 PACKET

    NDC Code 62003-422-04

    Package Description: 1 BOTTLE, PUMP in 1 CARTON / 113 mL in 1 BOTTLE, PUMP

    Product Details

    What is NDC 62003-422?

    The NDC code 62003-422 is assigned by the FDA to the product Tiger Balm Arthritis Rub which is a human over the counter drug product labeled by Prince Of Peace Enterprises, Inc.. The generic name of Tiger Balm Arthritis Rub is camphor (synthetic) and menthol. The product's dosage form is cream and is administered via topical form. The product is distributed in 2 packages with assigned NDC codes 62003-422-02 2 ml in 1 packet , 62003-422-04 1 bottle, pump in 1 carton / 113 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 Tiger Balm Arthritis Rub?

    Shake well before usingApply generously to affected areas and massage gently until cream is absorbed into the skinFor adults and children over 12, rub well on the affected area. Repeat 3-4 times daily For children 12 years of age or younger, consult a doctor before use.

    What are Tiger Balm Arthritis Rub 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.

    Which are Tiger Balm Arthritis Rub UNII Codes?

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

    • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
    • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
    • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
    • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)

    Which are Tiger Balm Arthritis Rub 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 Tiger Balm Arthritis Rub?

    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.

    [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.

    [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.

    [10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

    [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".