CLEAN RX- ethyl alcohol solution

Clean Rx by

Drug Labeling and Warnings

Clean Rx by is a Otc medication manufactured, distributed, or labeled by Quality Innovations Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Ethyl Alcohol 75%

Purpose

Antiseptic

Use

Helps decrease bacteria on skin. Recommended for repeated use.

Warnings

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

Do not apply

around eyes

When using this product

avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor

 If irritation or redness develop and conditions 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. Children must be supervised in use of this product.

Directions

pump as needed into your palmsand throughly spread on both the hands.

Other information

• Store at 20°C (68° to 77°F).
• May discolor fabrics

Inactive ingredients

acrlates/C10-30 alkyl acrylates crosspolymer, benzophenone-4, glycerin, tocopherol, water

Principal Display Panel

NDC: 74235-075-02

Clean RxTM 2 oz

A percentage of the proceeds from this product will be donated towards the coronavirus epidemic

HAND SANITIZER

Kills 99.999% of GERMS

With Moisturizer and Vitamin E

2 FL OZ (60 mL)

NDC: 74235-075-08

Clean RxTM 8 oz

A percentage of the proceeds from this product will be donated towards the coronavirus epidemic

HAND SANITIZER

Kills 99.999% of GERMS

With Moisturizer and Vitamin E

8 FL OZ (240 mL)

INGREDIENTS AND APPEARANCE

CLEAN RX 
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74235-750
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
SULISOBENZONE (UNII: 1W6L629B4K)
WATER (UNII: 059QF0KO0R)
TOCOPHEROL (UNII: R0ZB2556P8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74235-750-02	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020
2	NDC: 74235-750-08	240 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/07/2020

Labeler - Quality Innovations Inc. (079258818)

Registrant - Quality Innovations Inc. (079258818)