ECOFREAKS HAND SANITIZER SCENT FREE

ECOFREAKS FOAMING HAND SANITIZER SCENT FREE by

Drug Labeling and Warnings

ECOFREAKS FOAMING HAND SANITIZER SCENT FREE by is a Otc medication manufactured, distributed, or labeled by Sanitizer Supply, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ECOFREAKS FOAMING HAND SANITIZER SCENT FREE- benzalkonium chloride solution 
Sanitizer Supply, LLC

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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ECOFREAKS HAND SANITIZER

SCENT FREE

Drug Facts

Active Ingredients[s]

Benzalkonium chloride  0.13%

Purpose   Antiseptic

Use[s]

Hand sanitizer 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.

Do not use

• on 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.  These may be signs of a serious condition.

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Place enough product on hands to cover all surfaces.  Rub hands together until dry.
• 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  Water purified, Ethyl Alcohol, Sodium Lauryl Sulfate, Polyethylene Lauryl Ether, Aloe Vera, Hydrogen Peroxide 35%

ECOFREAKS FOAMING HAND SANITIZER SCENT FREE 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 90026-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
HYDROGEN PEROXIDE (UNII: BBX060AN9V)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
C12-16 PARETH-9 (UNII: 9DJ758090Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 90026-030-03	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2021
2	NDC: 90026-030-16	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2021
3	NDC: 90026-030-90	3785 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/19/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/19/2021	04/27/2022

Labeler - Sanitizer Supply, LLC (117594299)

Establishment
Name	Address	ID/FEI	Business Operations
Sanitizer Supply, LLC		117594299	manufacture(90026-030) , pack(90026-030) , label(90026-030)

Revised: 4/2022

Document Id: ddb8e74c-8f7e-b417-e053-2a95a90ad4a6

34390-5

Set id: ca43b635-e999-4547-9d0e-a4b4ca088117

Version: 2

Effective Time: 20220428