DOCTORS TOUCH Erase The Pain Lidocaine
DOCTORS TOUCH Erase The Pain Lidocaine is an FDA drug label for the active ingredient LIDOCAINE HYDROCHLORIDE manufactured by DOCTOR'S CHOICE MEDICAL, LLC 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 20231106.
Generic: LIDOCAINE HYDROCHLORIDE
Manufacturer: DOCTOR'S CHOICE MEDICAL, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 80045-400
Application: M015
Effective: 20231106
Active Ingredients: Active Ingredients Lidocaine HCL 4.00 % Purpose Topical Analgesic
Indications & Usage
Uses: For the temporary relief of pain.
Dosage & Administration
Directions: Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.
Contraindications
Not available.
Warnings
Warnings: not intended for ingestion. For external use only Do not use in large quantities, particularly over raw surfaces, or blistered areas. When using this product Avoid contact with the eyes. Avoid contact with the eyes. condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use
Adverse Reactions
Not available.
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