FQ Hand Sanitizer

Manufacturer
FQ Specialty Chemicals S.A. de C.V.
Effective date
2020-10-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:07:12

Label at a glance#

ProductFQ Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

• 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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 96° 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use[s]

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

When using this product:

OTC - WHEN USING SECTION

Avoid contact with eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or rash occurs.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

SPL UNCLASSIFIED SECTION

• Store between 15 – 30° C (59 –68°F)
• Avoid freezing
• Avoid excessive heat above 40°C (104°F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, emulsifiers.

Questions?

OTC - QUESTIONS SECTION

sales@fq-chem.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73584-00973584-009-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
e4a09b47-4371-1ea4-e053-2995a90af75ab2088931-6378-1cbf-e053-2a95a90a9b3f2022-07-25WarningsExact identifier
spl set id: b2088931-6378-1cbf-e053-2a95a90a9b3f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.