NDC product

Universal ARTHRITIS and SPORT

NDC 52000-301 · Universal Distribution Center LLC

Key facts

Product NDC 52000-301
Proprietary name Universal ARTHRITIS and SPORT
Nonproprietary name Methyl Salicylate, Capsicum
Substances METHYL SALICYLATE, CAPSICUM
Dosage form LIQUID
Route TOPICAL
Labeler Universal Distribution Center LLC
Product type HUMAN OTC DRUG
Marketing category OTC MONOGRAPH DRUG
Application number M017
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC] and 2 more
Marketing start Nov 1, 2023
Listing certified through Dec 31, 2026

At a glance

  • 1–9 Package NDCs

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About National Drug Codes (NDC)

The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.

Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date:

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