Active Ingredients
Benocaine 6%
Alcohol 60%
Sting Relief
FDA Label NDC 73659-006
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 73659-006). 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, use, warnings, do not use, stop use 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
First aid antiseptic
Use
- first aid to help prevent infection in minor scrapes
- for the temporary relief of itching insect bites
Warnings
For external use only
Do Not Use
- over large areas of the body
- in the eyse or apply
- over raw or blistered areas
Stop Use If:
- if conditions worsen or persists 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 a Poison Control right away.
Directions
- adults and children 2 years of age and older
- apply to cleaned affected area not more than 3 to 4 times daily.
- children under 3 years of age: consult a doctor
Other Information
stor at room temperaturel 15°-30° C (59°-86° F)
Inactive Ingredient
water
* Please review the disclaimer below.
