ALLPURE HAND SANITIZER- alcohol gel

ALLPURE HAND SANITIZER by

Drug Labeling and Warnings

ALLPURE HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by YESILILGAZ KOZMETIK KIMYA INSAAT OTOMOTIV VE GIDA SANAYI TICARET LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 70% v/v.

Purpose

Antiseptic

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

When using this products keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces.. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

Store above 15·30C (59·86F)

Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Carbomer, Glycerin, Purified Water, Rosmarinus Officinalis Extract, Triethanolamine

Product label

INGREDIENTS AND APPEARANCE

ALLPURE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78575-002
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
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
TROLAMINE (UNII: 9O3K93S3TK)
ROSEMARY (UNII: IJ67X351P9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78575-002-01	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020
2	NDC: 78575-002-02	50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020
3	NDC: 78575-002-03	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020
4	NDC: 78575-002-04	250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020
5	NDC: 78575-002-05	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020
6	NDC: 78575-002-06	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020
7	NDC: 78575-002-07	5000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/20/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	07/20/2020

Labeler - YESILILGAZ KOZMETIK KIMYA INSAAT OTOMOTIV VE GIDA SANAYI TICARET LIMITED SIRKETI (355436838)

Establishment
Name	Address	ID/FEI	Business Operations
YESILILGAZ KOZMETIK KIMYA INSAAT OTOMOTIV VE GIDA SANAYI TICARET LIMITED SIRKETI		355436838	manufacture(78575-002)