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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Health for the product Anti-itch Medicated Maximum Strength (NDC 69842-588). 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 other, active ingredient, purpose, use, warnings, stop use and ask doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Benzocaine 20%
Resorcinol 3%
External analgesic
External analgesic
temporarily relieves itching
For external use only
Allergy Allert
Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine or other –caine anesthetics.
Avoid contact with eyes
in case of contact rinse thoroughly and immediately with water.
condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days
If swallowed, get medical help or contact a Poison Control Center right away.
Adults and children 12 years and older
Apply a finger tip amount (approxiamtely a 1 inch strip) to the affected areas not more than 3 to 4 times daily
Children under 12 years
ask a doctor
questions?
Water, Mineral Oil, Cetyl Alcohol, Propylene Glycol, Glyceryl Stearate, PEG-100 Stearate, Isopropyl Palmitate, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Retinyl Palmitate, Zea Mays (Corn) Oil, Cholecalciferol, Lanolin Alcohol, Fragrance, Methylparaben, Carbomer, Isopropyl Myristate, Isopropyl Stearate, Sodium Sulfite, Triethanolamine, Trisodium EDTA, Maltodextrin
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