Active Inpradients
ETHYL BUTYLACETYLAMINOPROPIONATE 5%
Mosquito Repellent
FDA Label NDC 84445-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Furuizhilian Keji Co., Ltd. for the product Mosquito Repellent (NDC 84445-003). 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 inpradients, purpose, uses, warings, do not use, when using this product, stop use and ask a doctor if, 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
Insect Repellents
Uses
Make sure the application area is clean and dry.
Spray on the application area, be careful not to spray into the mouth or nose
Warings
Flammable, keep away from fire and flames.
For external use only
Do Not Use
on damaged skin
When Using This Product
Do not get into eyes.
If contact occurs, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation and redness develop. If condition persists more than 48 hours.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Use when going out or when there are many mosquitoes
Test on a small area before first use, and continue to use if there is no discomfort after 24 hours
Spray the area 2-3 times when using
Inactive Ingredient
Water, Alcohol Denat
* Please review the disclaimer below.
