KEEP IT CLEAN PURE CLEAN- alcohol solution

KEEP IT CLEAN by

Drug Labeling and Warnings

KEEP IT CLEAN by is a Otc medication manufactured, distributed, or labeled by G Mason Group LLC, 220 Laboratories Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ETHYL ALCOHOL 69%

PURPOSE

ANTISEPTIC

USES

TO DECREASE BACTERIA ON THE SKIN THAT COULD CAUSE DISEASE RECOMMENDED FOR REPEATED USE.

WARNINGS

For external use only: hands

Flammable. Keep away from fire or flame.

When using this product

• Keep out of eyes. In case of contact with eyes flush thoroughly with water.
• Avoid contact with broken skin.
• Do not ingest or inhale.

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.

• FOR CHILDREN UNDER 6, USE ONLY UNDER ADULT SUPERVISION.
• NOT RECOMMENDED FOR INFANTS.

OTHER INFORMATION

DO NOT STORE ABOVE 105 DEGREES F

• MAY DISCOLOR SOME FABRICS
• HARMFUL TO WOOD FINISHES AND PLASTICS

INACTIVE INGREDIENTS

WATER (AQUA), ALOE BARBADENSIS (ALOE VERA) LEAF JUICE, GLYCERIN, PROPYLENE GLYCOL, CARBOMER, PROPANDIOL, AMINOMETHYL PROPANOL, TOCOPHERYL ACETATE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KEEP IT CLEAN  PURE CLEAN
alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73389-103
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	69 mL  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
PROPANEDIOL (UNII: 5965N8W85T)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73389-103-11	236 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	03/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/17/2019

Labeler - G Mason Group LLC (078797167)

Establishment
Name	Address	ID/FEI	Business Operations
220 Laboratories Inc.		783247950	manufacture(73389-103)