Otc - Active Ingredient
Menthol 2%
Dch Pain Relieving Gel
FDA Label NDC 72839-031
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 Dch Pain Relieving (NDC 72839-031). 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
Topical Analgesic
Indications & Usage
For the temporary relief of minor aches and pains associated with arthritis, simple backache, strains, sprains, and bruises.
Warnings
For external use only.
Do not use with other topical pain relievers, with heating pad or heating devices.
When using this product do not use in or near the eyes, do not apply to wounds or damaged skin, do not bandage tightly.
Stop use and ask a doctor if condition worsens, symptoms last more than 7 days or clear and occur again within a few days.
Otc - Keep Out Of Reach Of Children
If product is swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
• adults and children 12 years and older, apply to affected area not more than 3 to 4 times daily. • Children under 12 years old, ask a doctor
Inactive Ingredient
Ammonium hydroxide, blue 1, carbomer, copper PCA, isopropyl alcohol, magnesium sulfate, sodium hydroxide, thymol, water.
* Please review the disclaimer below.
