Otc - Active Ingredient
Benocaine 6% lsopropyl Alcohol 70%
Sting Relief
FDA Label NDC 72766-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yangzhou Suxiang Medical Instrument Co., Ltd. for the product Sting Relief (NDC 72766-009). 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 otc - active ingredient, otc - purpose, uses, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Topical analgesic
antiseptic
Uses
For prevention of infection in minor scrapes andtemporary relief of itching insect bites
Warnings
For external use only.
Flammable, keep away from fire or flame.
Otc - Do Not Use
with electrocautery procedures.
In the eyes. If contact occurs, flush eyes with water.
Otc - Stop Use
Stop Use lf irritation and redness develop. If condition continues,consult your health care practitioner.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed,get medical help or contacta Poison Control Center right away.
Directions
Apply to affected area 3 or 4 times daily.
For adults and children 2 years of age and older.
Children under 2 years:consult physician.
Other Information
store at room temperature 15° - 30° C (59° - 86° F)
Inactive Ingredient
purified water
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Label (Label)
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