Active Ingredients
Benzocaine 6%
Stingx Swab
FDA Label NDC 65753-350
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Coretex Products Inc for the product Stingx (NDC 65753-350). 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, do not use, stop use and aska doctor if, 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
Use
For temporary pain relief from insect bites and stings
Warnings
For external use only
Do Not Use
- in or near eyes
- over large areas of the body
- over raw or blistered areas
Stop Use And Aska Doctor If
- conditions worsen or persist for more than 7 days or clear up and occur again within a few days
Keep Out Of Reach Of Children
If swallowed get medical help or contact Poison Control center right away.
Directions
Apply to affected area not more than 3 to 4 times daily, for adults and children 2 years of age or older.
Inactive Ingredients
SD alcohol 40, water (aqua), glycerin, allantoin
Other Safety Information
Made in USA for CoreTex Products, Inc.
Bakersfield, CA 93308
www.CoreTexProducts.com (877)684-5774
* Please review the disclaimer below.
