ALLPURE HAND SANITIZER SANITIZING WIPE- alcohol cloth

ALLPURE HAND SANITIZER SANITIZING WIPE by

Drug Labeling and Warnings

ALLPURE HAND SANITIZER SANITIZING WIPE by is a Otc medication manufactured, distributed, or labeled by CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Alcohol 70% v/v.

Purpose

Antiseptic

Use

Antiseptic wipe 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. Keep out of reach of children.

Do not use

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

WHEN USING

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

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

Glycerin, Butylene Glycol, Water, Lanolin

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

ALLPURE HAND SANITIZER SANITIZING WIPE 
alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 80176-001
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
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
LANOLIN (UNII: 7EV65EAW6H)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 80176-001-01	1 in 1 PACKET	08/20/2020
1		5 mL in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 80176-001-02	10 in 1 PACKET	08/20/2020
2		5 mL in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 80176-001-03	50 in 1 PACKET	08/20/2020
3		5 mL in 1 POUCH; Type 0: Not a Combination Product
4	NDC: 80176-001-04	72 in 1 PACKET	08/20/2020
4		5 mL in 1 POUCH; Type 0: Not a Combination Product
5	NDC: 80176-001-05	120 in 1 PACKET	08/20/2020
5		5 mL in 1 POUCH; Type 0: Not a Combination Product
6	NDC: 80176-001-06	200 in 1 PACKET	08/20/2020
6		5 mL in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	08/20/2020

Labeler - CERCI KOZMETIK VE OTEL EKIPMANLARI PAZARLAMA IC VE DIS TICARET LIMITED SIRKETI (502990784)