Hanzol Antiseptic Hand Sanitizer Gel

Manufacturer
Plymouth Technology, Inc.
Effective date
2020-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:14:38

Label at a glance#

ProductHanzol Gelled Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30° C (59-86° F)  • avoid freezing and excessive heat above 40° C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin

• recommended for repeated use

• for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire/flame 

For external use only

Do not use

• in children less than 2 months of age

• on open skin wounds

When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor if

• irritation and redness develop

• condition persists for more than 72 hours 

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

• wet hands thoroughly with product and allow to dry without wiping

• supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30° C (59-86° F) 

• avoid freezing and excessive heat above 40° C (104°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients  carbomer, fragrance, glycerin, hydrogen peroxide, sodium hydroxide, water

OTC - QUESTIONS SECTION

Questions? 1-248-537-0081

You may also report serious side effects to this phone number.

Mon- Fri 9:00AM - 5.00PM

SPL UNCLASSIFIED SECTION

Alcohol Antiseptic 70%

Topical Solution

Non-Sterile Solution

FLAMMABLE LIQUID

Ground/bond container and receiving equipment.

Use explosion-proof electrical/ventilating/light/equipment.

Use only non-sparking tools.

Take precautionary measures against static discharge.

Do not breathe dust/fume/gas/mist/vapors/spray.

Avoid breathing dust/fume/gas/mist/vapors/spray.

Wash face,hands, and any exposed skin thoroughly after handling.

Do not eat, drink or smoke when using this product.

Use only outdoors or in a well-ventilated area.

Wear protective gloves/protective clothing/eye protection/face protection

IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water [or shower].

IF INHALED:Remove person to fresh air and keep at rest in a position comfortable for breathing.

Store in a well-ventilated place. Keep container tightly closed.

Dispose of contents/container in accordance with local/regional/national/international regulations.

DOT CLASSIFICATION

UN1170, Flammable liquid, n.o.s.(ethanol), 3, II Lot Number:

MADE IN USA

Manufactured by: Plymouth Technology, Inc, 2700 Bond St, Rochester Hills, MI 48309

EMERGENCY TELEPHONE NO.

INFOTRAC (800) 535-5053

www.ptiwater.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76917-074-01HanzolGelled Hand Sanitizer3.8 L in 1 JUGGEL3.81
76917-074-05HanzolGelled Hand Sanitizer18.9 L in 1 CONTAINERGEL18.91
76917-074-55HanzolGelled Hand Sanitizer208.2 L in 1 DRUMGEL208.21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76917-074HANZOL GELLED HAND SANITIZER (ETHYL ALCOHOL) GEL [PLYMOUTH TECHNOLOGY, INC.]1Legacy NDC, 3 package rows20200527_0918346f-9202-40ee-8a2c-762597f5f1f1.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76917-07476917-074-01, 76917-074-05, 76917-074-55

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
2478b4f6-9139-41cd-b7f8-27af921d20340918346f-9202-40ee-8a2c-762597f5f1f12020-05-22WarningsExact identifier
spl id: 2478b4f6-9139-41cd-b7f8-27af921d2034
spl set id: 0918346f-9202-40ee-8a2c-762597f5f1f1

Reported adverse events (FAERS/openFDA)#

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