ABUTOL PARIS ANTISEPTIC HAND SANITIZER- ethyl alcohol gel

Abutol PARIS ANTISEPTIC HAND SANITIZER by

Drug Labeling and Warnings

Abutol PARIS ANTISEPTIC HAND SANITIZER 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 70%

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

Flammable, keep away from fire / flame
For external use only

Do not use in children less than 2 months of age
on open skin wounds
When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water. Do not inhale or ingest.

Stop and ask doctor if
irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

wet hands thoroughly with product and allow to dry without wiping
supervise children under 6 years of age when using this product to avoid swallowing

Other information

store between 15-30°C (59-86°F)
avoid freezing and excessive heat above 40°C (104°F)
may discolor certain fabrics or surfaces

Inactive ingredients 

carbomer, FD&C Blue No.1 , FD&C Yellow No.5, fragrance, glycerin, triethanolamine, water.

SPL UNCLASSIFIED SECTION

Distributed by: Daisy Distribution LLC, Wood Ridge, NJ 07075
Country Of Origin: Turkey

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

Lot No: 200620
Exp. Date: 06-2023
NDC: 77418-102-10

661799958882

No Rinsing Required
Does Not Dry The Skin

ALCOHOL CONTENT 70%

Packaging

INGREDIENTS AND APPEARANCE

ABUTOL PARIS ANTISEPTIC HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77418-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77418-102-10	1 in 1 CARTON	06/08/2020
1		80 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/08/2020

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(77418-102)