52000-072 NDC - MUSCLE RUB PAIN RELIEVER GEL ()

Drug Information

  • Product NDC: 52000-072
  • Proprietary Name: Muscle Rub Pain Reliever Gel
  • Non Proprietary Name:
  • Active Ingredient(s): 25 mg/g MENTHOL, UNSPECIFIED FORM
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Universal Distribution Centre LLC
Product Type:
FDA Application Number: M017
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/24/2021

Package Information

No. Package Code Package Description Billing Unit
152000-072-021 TUBE in 1 CARTON (52000-072-02) / 35.4 g in 1 TUBE (52000-072-01)
252000-072-041 TUBE in 1 CARTON (52000-072-04) / 35.4 g in 1 TUBE (52000-072-03)

NDC Record

Field Name Field Value Definition
PRODUCT NDC52000-072The 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.
PROPRIETARY NAMEMuscle Rub Pain Reliever GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/24/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM017This 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 NAMEUniversal Distribution Centre LLCName of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC52000-072The 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.
PROPRIETARY NAMEMuscle Rub Pain Reliever GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/24/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM017This 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 NAMEUniversal Distribution Centre LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/19/2025

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