Hand Sanitizer Gel

Manufacturer
SPIRIT PHARMACEUTICALS LLC
Effective date
2022-12-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:52:02

Label at a glance#

ProductHand Sanitizer Gel
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

• hand sanitizer to help reduce bacteria on the skin that potentially can cause disease • recommend for repeated use

Dosage and administration

    Place enough product on hands to cover all surfaces. Rub hands together until dry.    Children under 6 years of age should be supervised when using this product

Storage and handling

• Store between 15°-30°C (59°86°F) • Avoid freezing and excessive heat above 40°C (104°F) • may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to help reduce bacteria on the skin that potentially can cause disease
• recommend for repeated use

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat and flame.
Do not use • in 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 appears and lasts. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  •     Place enough product on hands to cover all surfaces. Rub hands together until dry.
  •    Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

• Store between 15°-30°C (59°86°F)
• Avoid freezing and excessive heat above 40°C (104°F)
• may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzalkinium chloride, fragrance, glycerin, hydrogen peroxide, isopropyl myristate, propylene glycol, tocopheryl acetate, water

Questions or comments?

OTC - QUESTIONS SECTION

1-888-333-9792

SPL UNCLASSIFIED SECTION

Manufactured by: APL

P.O. Box 7771, Ajman, UAE

Under License From

MODD PERFUMES & COSMETICS

10 Cameron Road, Seven Kings

London, IG3 8LA

United Kingdom

For external use only

Made in U.A.E.

Distributed By:

Spirit Pharamceuticals LLC

Ronkonkoma, NY 11779

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HANDY

HAND-SANITIZER SOLUTION

EFFECTIVELY KILLS 99.9% OF THE

MOST COMMON GERMS/ BACTERIA

70%

ALCOHOL CONTENT

WITH

VITAMIN E & MOISTURIZERS

PLEASANT FRAGRANCE

STAY PROTECTED

16.9 FL. OZ. (500 ml)

MODD

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN4
582753ethanol 0.7 ML/ML Topical SolutionSCD4
582753ethanol 70 % Topical SolutionSY4
582753ethyl alcohol 70 % Topical SolutionSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68210-4082-52024-01-30C16284748780-11030e365-0fd1-111a-e063-dadaa90a10e2HAND SANITIZER SOLUTION

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68210-4082-5Hand Sanitizer Gel500 mL in 1 BOTTLESOLUTION5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68210-4082HAND SANITIZER GEL (ETHYL ALCOHOL) SOLUTION [SPIRIT PHARMACEUTICALS LLC]4Legacy NDC, 1 package rows20221206_419bfa23-6958-440c-88fc-5da9c94cd6f1.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68210-408268210-4082-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

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
ef1ad8bb-319a-14bc-e053-2995a90ab192419bfa23-6958-440c-88fc-5da9c94cd6f12022-12-05WarningsExact identifier
spl id: ef1ad8bb-319a-14bc-e053-2995a90ab192
spl set id: 419bfa23-6958-440c-88fc-5da9c94cd6f1

Reported adverse events (FAERS/openFDA)#

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