Active Ingredients
Benocaine 6%
SD Alcohol 60%
Sting Relief
FDA Label NDC 73659-006
10 label sections · Submitted to the FDA by Rapid Care, Inc · 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 73659-006). 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, uses, warnings, warnings and precautions, do not use in eyes, 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
Purpose
Topical analgesic
First aid antiseptic
Uses
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.
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
water
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