FQ Hand Sanitizer by FQ Specialty Chemicals S.A. de C.V. FQ Hand Sanitizer

FQ Hand Sanitizer by

Drug Labeling and Warnings

FQ Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by FQ Specialty Chemicals S.A. de C.V.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FQ HAND SANITIZER- alcohol gel 
FQ Specialty Chemicals S.A. de C.V.

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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FQ Hand Sanitizer

Drug Facts

Active Ingredient

Ethyl Alcohol 96° 70%

Purpose

Antiseptic

Use[s]

Health care personnel hand rub to reduce microorganisms that potentially can cause disease.

Warnings

For external use only. Flammable. Keep away from heat of flame.

Do not use

in children less than 2 months of age
on open skin wounds

When using this product:

Avoid contact with 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.

Keep out of reach of children

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

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 – 30° C (59 –68°F)
Avoid freezing
Avoid excessive heat above 40°C (104°F).

Inactive Ingredients

Purified Water, emulsifiers.

Questions?

sales@fq-chem.com

Package Labeling:

FQ HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73584-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 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: 73584-009-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/15/2020	11/03/2021

Labeler - FQ Specialty Chemicals S.A. de C.V. (812744112)

Revised: 7/2022

Document Id: e4a09b47-4371-1ea4-e053-2995a90af75a

34390-5

Set id: b2088931-6378-1cbf-e053-2a95a90a9b3f

Version: 2

Effective Time: 20220725