Drug Information

Product NDC: 66761-322

Proprietary Name: Tiger Balm

Non Proprietary Name: Camphor (Synthetic), Menthol, and Capsicum

Active Ingredient(s):
  • 80 mg/1 CAMPHOR (SYNTHETIC);
  • 16 mg/1 CAPSICUM

Administration Route(s): TOPICAL

Dosage Form(s): PATCH

Labeler Information

Labeler Name: Haw Par Healthcare Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part348
Start Marketing Date:11/15/2001

Package Information

No. Package Code Package Description Billing Unit
166761-322-0136 PACKET in 1 BOX (66761-322-01) > 1 PATCH in 1 PACKET
266761-322-0236 PACKET in 1 BOX (66761-322-02) > 1 PATCH in 1 PACKET
366761-322-051 PACKET in 1 BOX (66761-322-05) > 5 PATCH in 1 PACKET
466761-322-1212 PACKET in 1 BOX (66761-322-12) > 1 PATCH in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC66761-322The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMETiger BalmThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECamphor (Synthetic), Menthol, and CapsicumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPATCHThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/15/2001This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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.
APPLICATION NUMBERpart348This 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.
LABELER NAMEHaw Par Healthcare Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMECAMPHOR (SYNTHETIC); MENTHOL, UNSPECIFIED FORM; CAPSICUMThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE INGRED UNITmg/1; mg/1; mg/1 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 1/24/2020