JUMBO WIPES- ethyl alcohol, isopropyl alcohol cloth

Jumbo Wipes by

Drug Labeling and Warnings

Jumbo Wipes by is a Otc medication manufactured, distributed, or labeled by QUIKIT LIMITED. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Isopropyl alcohol 3.75%

Ethyl alcohol 71.25%

Purpose

Antiseptic.

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 product 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. 

Uses

Hand sanitiser wipe to decrease bacteria on the skin that could cause disease.

Use when soap and water are not available.

Directions

• Pull cloth our of opening & wipe hands thoroughly. 
• Discard used wipe in trash receptacle, do not flush. 
• Children under 6 years of age should be supervised when using this product. 
• Close package after each us.

Keep out of reach of children.

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

Other information

Do not store above 115°F

May discolor some fabrics

May damage wood finishes

Inactive Ingredients

Purified Water

Product Image

INGREDIENTS AND APPEARANCE

JUMBO WIPES 
ethyl alcohol, isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81071-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71.25 mL  in 100 mL
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	3.75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81071-001-01	250 in 1 PACKAGE	11/15/2020
1		2.07 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
2	NDC: 81071-001-02	500 in 1 PACKAGE	11/15/2020
2		2.07 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
3	NDC: 81071-001-03	800 in 1 PACKAGE	11/15/2020
3		2.07 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
4	NDC: 81071-001-04	1000 in 1 PACKAGE	11/15/2020
4		2.07 mL in 1 NOT APPLICABLE; Type 0: Not a Combination Product
5	NDC: 81071-001-05	1200 in 1 PACKAGE	11/15/2020
5		2.07 mL in 1 NOT APPLICABLE; 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	11/15/2020

Labeler - QUIKIT LIMITED (223528184)