Active Ingredients
Benzocaine, 6% w/v
Sting Relief Wipes Swab
FDA Label NDC 58228-2204
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prostat First Aid Llc for the product Sting Relief Wipes (NDC 58228-2204). 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 active ingredients, purpose, active ingredient, use(s), warnings, when using, do not use, stop use if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Antiseptic
Active Ingredient
Isopropyl Alcohol, 60% w/v
Use(S)
For the temporary relief of pain and/or itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations
Warnings
For External Use Only
Flammable. Keep away from fire or flame.
When Using
• Avoid contact with eyes; if this occurs, rinse thoroughtly with water
Do Not Use
• With electrocautery procedures
Stop Use If
• Irritation and redness develop
• Condition worsens or symptoms persist for more than 7 days, or clear up and occur again within a few day; discontinue use and consult a doctor
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
• For adults and children 2 years of age and older, apply to affected area not more than 3-4 times daily.
• For children under 2 years of age, consult a doctor before use.
Other Information
• Store at room temperature 15°-30°C (59°-86°F)
• Avoid excessive heat
Inactive Ingredients
Water
Questions And Comments?
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Label
Ps-2204_bx_master (Ps 2204 Bx Master R231103 2)
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