HEXADERMAL ANTISEPTIC HAND SANITIZER

HEXADERMAL ANTISEPTIC HAND SANITIZER by

Drug Labeling and Warnings

HEXADERMAL ANTISEPTIC HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by KUZEY SAGLIK URUNLERI VE KIMYA SANAYI ANONIM SIRKETI KAZAN SUBESI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HEXADERMAL ANTISEPTIC HAND SANITIZER- alcohol gel 
KUZEY SAGLIK URUNLERI VE KIMYA SANAYI ANONIM SIRKETI KAZAN SUBESI

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HEXADERMAL ANTISEPTIC HAND SANITIZER

Drug Facts

Active ingredient

Ethyl alcohol 72%

Purpose

Antiseptic

Use

for hand washing to decrease bacteria on the skin

Warnings

For externale use only. Flammable. keep away from fire or flame.

Do not use

in the eyes.

Stop use and ask a 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

Other information

Store below 110°F (43°C)

Inactive ingredients

Aminomethylpropanol, Carbomer, Fragrance, Glycerin, Isopropyl Alcohol, Water.

Package Labeling:500ml

Package Labeling:250ml

Package Labeling:100ml

HEXADERMAL ANTISEPTIC HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80256-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.72 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80256-000-00	100 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/31/2020	09/05/2024
2	NDC: 80256-000-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/31/2020	09/05/2024
3	NDC: 80256-000-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/31/2020	09/05/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	07/31/2020	09/05/2024

Labeler - KUZEY SAGLIK URUNLERI VE KIMYA SANAYI ANONIM SIRKETI KAZAN SUBESI (519910295)

Establishment
Name	Address	ID/FEI	Business Operations
KUZEY SAGLIK URUNLERI VE KIMYA SANAYI ANONIM SIRKETI KAZAN SUBESI		519910295	manufacture(80256-000)

Revised: 9/2024

Document Id: 21752509-8cb0-5157-e063-6394a90a5f1f

34390-5

Set id: ffd9ead9-2710-4c1b-87ba-261a6fded1be

Version: 4

Effective Time: 20240906

 

KUZEY SAGLIK URUNLERI VE