Active Ingredients
Benocaine 6%
Isoproyl Alcohol 70%
Sting Relief
FDA Label NDC 73659-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rapid Care, Inc for the product Sting Relief (NDC 73659-009). 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 active ingredients, purpose, use, warnings, warnings and precautions, do not use in eyes, stop use, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical analgesic
Antiseptic
Use
First aid to help prevent infection in minor scrapes and temporary relief of itching insect bites
Warnings
For external use only.
Warnings And Precautions
Flammable, keep away from fire or flame.
Do Not Use In Eyes
, broken skin, deep punture wounds, or if unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately.
Stop Use
if irritation and redness develop. If condition continues, consult your heath care practitioner.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control right away.
Directions
Apply to affect area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician.
Other Information
store at room temperature 15° - 30° C (59° - 86° F)
Inactive Ingredient
purified water
* Please review the disclaimer below.
