TARGOL SANITIZING FRESH LINEN- ethyl alcohol aerosol, spray

TARGOL Sanitizing Fresh Linen by

Drug Labeling and Warnings

TARGOL Sanitizing Fresh Linen by is a Otc medication manufactured, distributed, or labeled by HEDEF KIMYA SANAYI VE TICARET ANONIM SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 75% v/v

Purpose

Antiseptic

Use:

Effective in destroying (harmful) bacteria to provide antiseptic cleansing.

Warning

For external use only. Do not swallow. Do not inhale.

CONTAINER MAY EXPLODE IF HEATED. Do not use in presence of open flame or spark. Contents under pressure. Do not place in hot water or near radiators, stoves or other sources of heat. Do not puncture or incinerate container or store at temperatures over 50°C (122°F).

FIRST AID TREATMENT: When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water for at least 20 minutes.

Stop use and ask/ consult a doctor/ physician/ health care practitioner/ health care provider/ health care professional if irritation develops.

Keep out of reach of children. If swallowed, call a poison control centre or get medical help right away.

Directions:

Adults and children over 2 years of age. Supervise children when they use this product. For occasional and personal domestic use. Shake well before using. Hold can upright and spray 6-8 inches away evenly.

Other information

Lot No. and Expiration Date can be found on container.

Inactive ingredients

Ethanol (Éthanol), Butane, Propane, Isobutane, Parfum.

SPL UNCLASSIFIED SECTION

KILLS 99.9% of Most Common Germs

Fresh Linen

SCENT/PARFUM

CONTAINS 75% ALCOHOL

DANGER

EXTREMELY FLAMMABLE

CONTAINER MAY EXPLODE IF HEATED

Read precautions on back panel.

Quick & Effective

Eliminates Odors

Fights the Spread of Germs

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

Packaging

INGREDIENTS AND APPEARANCE

TARGOL SANITIZING FRESH LINEN 
ethyl alcohol aerosol, spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80793-011
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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80793-011-01	550 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/27/2020
2	NDC: 80793-011-02	600 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	11/27/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/27/2020

Labeler - HEDEF KIMYA SANAYI VE TICARET ANONIM SIRKETI (552244873)

Establishment
Name	Address	ID/FEI	Business Operations
HEDEF KIMYA SANAYI VE TICARET ANONIM SIRKETI		552244873	manufacture(80793-011)