Easy Klean Ethyl Alcohol by Frenda Corporation Easy Klean Ethyl Alcohol

Easy Klean Ethyl Alcohol by

Drug Labeling and Warnings

Easy Klean Ethyl Alcohol by is a Otc medication manufactured, distributed, or labeled by Frenda Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

EASY KLEAN ETHYL ALCOHOL- alcohol liquid 
Frenda Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Easy Klean Ethyl Alcohol

Drug Facts

Active Ingredient

Ethyl Alcohol 75%

Purpose

First aid antiseptic

USE

helps prevent the risk of infections in minor cuts, scrapes and burns

Warnings

For external use only.

Flammable. keep away from fire or flame, heat spark, electrical

USE ONLY IN A WELL-VENTILATED AREA; FUMES MAY BE HARMFUL

Ask doctor before use

for deep wounds, animal bites or serious burns

Whem using this product

• do not get in to eyes
• do not apply over large areas of the body
• do not use longer tham 1 week

Stop use and ask a doctor if

the condition persists or gets worse

Keep out of the reach of children.

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

Directions

• clean affected areas
• apply 1 to 3 times daily

Inactive ingredients

Softened Water

Other information:

store at controlled room temperature 

• will produce serius gastric disturbances if taken internally

Package Labeling: 74115-003-10

Package Labeling: 74115-003-34

EASY KLEAN ETHYL ALCOHOL 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74115-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 mL  in 1 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74115-003-10	296 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020	03/31/2022
2	NDC: 74115-003-34	1005 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2020	03/31/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	04/25/2020	03/31/2022

Labeler - Frenda Corporation (141588629)

Establishment
Name	Address	ID/FEI	Business Operations
Frenda Corporation		141588629	manufacture(74115-003)

Revised: 3/2023

Document Id: f655c6fa-56e2-19b8-e053-2995a90a4241

34390-5

Set id: a74a1929-b05e-4125-982b-e67552a63042

Version: 2

Effective Time: 20230307