TARGOL SANITIZING- ethyl alcohol aerosol, spray

Targol by

Drug Labeling and Warnings

Targol by is a Otc medication manufactured, distributed, or labeled by Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl alcohol 75%

Purpose

Antiseptic

Uses

hand sanitizer to decrease bacteria on the skin

recommended for repeated use

for use when soap and water are not available

Warnings

Extremely flammable aerosol, keep away from fire / flame.

Keep away from heat, hot surfaces, open flames and other ignition sources.

Pressurized container. Do not pierce or burn even after use.

Protect from the sunlight.

For external use only.

Do not use

on children less than 2 months of age

on open skin wounds

When using this product Avoid use on/or around eyes, ears, mouth, broken/irritated skin or large areas of body. In case of contact with eyes, rinse thoroughly with water several minutes. do not inhale or ingest.

Stop and ask doctor if

irritation persist

or if product is swallowed

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions

Shake well before use.

Hold can upright at 6-7 inches away from surface and spray evenly.

Allow to air dry for 5 to 10 minutes. Repeat application a necessary

Supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-30°C (59-86°F)

Do not expose to temperatures exceeding 50 C/122 F.

INACTIVE INGREDIENT

Inactive ingredients Butane, Propane, Isobutane, Parfum, glycerin

SPL UNCLASSIFIED SECTION

Kills 99.9% of Most Common Germs*

JASMINE

ALCOHOL CONTENT 75 %

Sanitizer Spray

*Effective at eliminating 99.9% of many common harmful germs and bacteria in as little as 15 seconds

You may also report any serious side effects to P O Box 328, Wood Ridge, NJ 07075-328

Packaging

INGREDIENTS AND APPEARANCE

TARGOL  SANITIZING
ethyl alcohol aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78089-036
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BUTANE (UNII: 6LV4FOR43R)
PROPANE (UNII: T75W9911L6)
ISOBUTANE (UNII: BXR49TP611)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78089-036-01	550 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	09/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	09/07/2020

Labeler - Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi (565678914)

Establishment
Name	Address	ID/FEI	Business Operations
Endeks Kimya Sanayi Ve Ticaret Anonim Sirketi		565678914	manufacture(78089-036)