Sting Relief Solution
FDA Label NDC 72459-016
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yiwu Ori-power Medtech Co.,ltd. for the product Sting Relief (NDC 72459-016). 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 drug facts, active ingredients, purpose, inactive ingredients, use, directions, storage, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
Benzocaine 6% w/v, Isopropyl Alcohol 60% w/v
Purpose
For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites.
Inactive Ingredients
Purified Water, Sodium Bicarbonate.
Use
Temporary relief for minor burns, scrapes and insect bites.
Directions
Apply to affected area no more than 3 to 4 times daily. For children under 2 years of age, consult physician before use.
Storage
Store at room temperature 15°C - 30°C (59°F - 86°F).
Warnings
Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If irritation develops, consult physician. Do not use on broken skin, deep puncture wounds.
Keep Out Of Reach Of Children
In case of accidental swallowing, seek medical help and contact poison control immediately.
Do Not Use
on broken skin, deep puncture wounds.
Package Labeling:
Label2 (Label2)
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