Otc - Active Ingredient
Lidocaine 4%, Menthol 1%
Dch Nerve Pain Relief Spray
FDA Label NDC 72839-223
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 Nerve Pain Relief (NDC 72839-223). 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 anesthetic, Topical analgesic
Indications & Usage
Temporarily relieves minor pain
Warnings
For external use only.
Flammable--Keep away from fire or flame.
Do not use if you have had an allergic reaction to lidocaine or other local anesthetics, on large areas of he body or on cut, irritated, blistered or swollen skin, on puncture wounds, for more than one week without consulting a doctor.
When using this product only use as directed, avoid contact with eyes and mucous membranes, rare cases of serious burns have been reported with products of this type, do not apply to wounds or damaged, broken, or irritated skin, do not bandage tightly or apply local heat (such as heating pads) or a medicated path to the area of use, a transient burning sensation may occur upon application but generally disappears in several days, avoid applying into skin folds.
Stop use and ask a doctor if condition worsens, severe burning sensation, redness, rash or irritation develops, symptoms persist for more than 7 days or clear up and occur again within a few days, you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.
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Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
When practical, cleanse the affected area with mild soap and warm water, Rinse thoroughly and gently pat dry. Spray affected area. Wash hands after applying. Adults and children 2 years of age and older, apply externally to the affected area up to 6 times a day. Children under 12 years of age: consult a doctor.
Inactive Ingredient
Alcohol denat., caprylic/capric triglyceride, propylene glycol, arnica montana flower extract, anthemis nobilis flower oil, aloe barbadensis leaf extract, eucalyptus globulus leaf oil.
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