ABUTOL SANITIZING WATERFALL- ethyl alcohol spray

Abutol Sanitizing Waterfall by

Drug Labeling and Warnings

Abutol Sanitizing Waterfall by is a Otc medication manufactured, distributed, or labeled by ATAK FARMA KOZMETIK VE KIMYA SANAYI 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/122F.

Inactive ingredients

Butane, Propane, Isobutane, Glycerin, Parfum

SPL UNCLASSIFIED SECTION

KILLS 99.9% OF VIRUSES BACTERIA*

ALCOHOL CONTENT 75%

*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 PO Box 328, Wood Ridge, NJ 07075-328

Made in TURKEY

Packaging

INGREDIENTS AND APPEARANCE

ABUTOL SANITIZING WATERFALL 
ethyl alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77418-302
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: 77418-302-50	550 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/23/2020

Labeler - ATAK FARMA KOZMETIK VE KIMYA SANAYI TICARET ANONIM SIRKETI (566218248)

Establishment
Name	Address	ID/FEI	Business Operations
ATAK FARMA KOZMETIK VE KIMYA SANAYI TICARET ANONIM SIRKETI		566218248	manufacture(77418-302)