San-EZ Hand Sanitizer - Gel

Manufacturer
Dental Technologies, Inc.
Effective date
2025-11-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:42:01

Label at a glance#

ProductSan-EZ Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

Hand sanitizer to help reduce microbes that potentially can cause disease. For use when soap and water are not available.

Dosage and administration

Place enough product on hand 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

70% v/v Ethyl Alcohol

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce microbes that potentially can cause disease.

  • For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if irritation or rash occures. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hand 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

OTHER SAFETY INFORMATION

  • Store between 15-30ºC (59-86ºF)
  • Avoid freezing and excessive heat above 40ºC (104ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Carbomer, Fragrance, Aminomethyl Propanol

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-835-0885

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SAN-EZ™

Gel

Hand Sanitizer

Essened with Aloe & Shea

8 fl. oz. (236mL)

REF 033.0202.002

PM5629 REV.000.jpgPM5629 REV.000.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130868824000060GTIN-13: 0868824000060
EAN-13: 0868824000060
GTIN-12: 868824000060
UPC-A: 868824000060
GTIN storage (14 digits): 00868824000060
PM5629 Rev.000.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55346-3302-1San-EZ Hand Sanitizer236 mL in 1 BOTTLE, PLASTICGEL2363

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55346-330255346-3302-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22024-12-20full-release2026-06-01 00:47:42

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
San-EZ Hand SanitizerETHYL ALCOHOL 70%Dental Technologies, Inc.a2cca707-103d-7265-e053-2995a90aebfc2025-11-04WarningsExact identifier
ndc (package): 55346-3302-1
ndc (product): 55346-3302
ndc11 (package): 55346330201
spl id: 42c8670e-5fbc-736d-e063-6394a90a2b51
spl set id: a2cca707-103d-7265-e053-2995a90aebfc

Reported adverse events (FAERS/openFDA)#

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