United States · FDA National Drug Code directory

DynaRub

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
67777-113_275e9d16-0717-f77a-e063-6394a90abb49
Product NDC
67777-113
Form
CREAM
Composition / generic term
Pain Relieving Cream
Labeler
Dynarex Corporation
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20160912
Source listing expiry
20261231

Source-listed ingredients

  • MENTHOL — 10 g/100g
  • METHYL SALICYLATE — 15 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 72 TUBE in 1 CASE (67777-113-50) / 85 g in 1 TUBE (67777-113-49) · 67777-113-50

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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DynaRub — United States | Molindra Medicines