Otc - Active Ingredient
Menthol 8%, Methyl Salicylate 30%
Dr Goldsons Pain Cream
FDA Label NDC 72839-145
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Derma Care Research Labs, Llc for the product Dr Goldsons Pain (NDC 72839-145). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
External Analgesic
Indications & Usage
For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.
Warnings
For external use only. Do not use on wounds or damaged skin or with a heating pad. When using this product avoid contact with eyes or mucous membranes, do not bandage tightly. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days, excessive skin irritation occurs.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Use only as directed. Adults and children over 12 years: apply to affected area not more than 3 to 4 times daily. Children 12 years oryounger: ask a doctor. Close cap tightly after use.
Inactive Ingredient
Water, lanolin, glyceryl stearate SE, stearic acid, polysorbate 80, curcuma longa (turmeric) root extract, glycerin, carbomer, triethanolamine, potassium hydroxide, disodium EDTA
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