MOSQUITO REPELLENT- ethyl butylacetylaminopropionate liquid

MOSQUITO REPELLENT by

Drug Labeling and Warnings

MOSQUITO REPELLENT by is a Otc medication manufactured, distributed, or labeled by Shenzhen Furuizhilian keji Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active inpradients

ETHYL BUTYLACETYLAMINOPROPIONATE 5%

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MOSQUITO REPELLENT 
ethyl butylacetylaminopropionate liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84445-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ETHYL BUTYLACETYLAMINOPROPIONATE (UNII: 65GQA237EH) (ETHYL BUTYLACETYLAMINOPROPIONATE - UNII:65GQA237EH)	ETHYL BUTYLACETYLAMINOPROPIONATE	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84445-003-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	07/11/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/11/2024

Labeler - Shenzhen Furuizhilian keji Co., Ltd. (418598613)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Furuizhilian keji Co., Ltd.		418598613	manufacture(84445-003)