Totally Fun After Sun
Totally Fun After Sun is an FDA drug label for the active ingredient LIDOCAINE HCL manufactured by MJ Products Association, 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 20231115.
Generic: LIDOCAINE HCL
Manufacturer: MJ Products Association, LLC
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 72085-145
Application: M017
Effective: 20231115
Active Ingredients: Active Ingredients Lidocaine HCL 1.50% PURPOSE Topical Anesthetic
Indications & Usage
Indications For the Temporary relief of pain and itching due to sunburn, minor skin irritations, minor cuts, minor burns, scrapes and insect bites.
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.
Contraindications
Not available.
Warnings
WARNINGS FOR EXTERNAL USE ONLY Do not use in large quantites, particularly over raw or blistered areas. Avoid contact with eyes. Stop use and ask a doctor if condition gets worse, symptoms last for more than 7 days, or symptoms clear up and occur again with a few days. If sumptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician.
Adverse Reactions
Not available.