INSTA RELIEF DM

LIDOCAINE HYDROCHLORIDE, MENTHOL TOPICAL HUMAN OTC DRUG

INSTA RELIEF DM is an FDA drug label for the active ingredient LIDOCAINE HYDROCHLORIDE, MENTHOL manufactured by DM LAB CORP administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231105.

Generic name
LIDOCAINE HYDROCHLORIDE, MENTHOL
Manufacturer
DM LAB CORP
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
72465-600
Application
M017
Label effective
20231105

Active ingredients

ACTIVE INGREDIENTS Lidocaine HCL 4.00% Menthol 1.00% Topical Anesthetic

Indications & Usage

INDICATIONS: For the temporary relief of pain and itching assoicated with minor burns sunburn, minor cuts, scrapes, insect bites or minor skin irritations.

Dosage & Administration

DIRECTIONS: Adults and children two-years of age or older: Apply to affected area not more than three to four times daily Children under two-years of age: consult a physician.

Warnings

WARNINGS For external use only. Avoid contact with eyes. If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not apply to wounds or damaged skin. Do not bandage tightly. If pregnant or breast feeding, contact physician

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