DMC GEL ANTIBACTERIAL HAND SANITIZING GEL (62172-118)

Manufacturer
DIVERSIFIED MANUFACTURING CORP
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:13:18

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

KILLS 99.99% OF GERMS. ANTISEPTIC HAND RUB.

Dosage and administration

Put small amount into palm of hand. Rub together until dry.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL (62.0%)

PURPOSE

OTC - PURPOSE SECTION

SANITIZER

USES

INDICATIONS & USAGE SECTION

KILLS 99.99% OF GERMS.

ANTISEPTIC HAND RUB.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY.

* DO NOT GET INTO EYES.
* FLAMMABLE - Do not use near heat, fire, flame or while smoking. In case of eye contact, flush immediately and thoroughly with water.


OTC - KEEP OUT OF REACH OF CHILDREN SECTION

* KEEP OUT OF REACH OF CHILDREN. * Do not ingest. If swallowed, seek medical help or call poison control immediately.

* Stop use and ask a doctor if redness and/or irritation occurs and stays longer than 7 days.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Put small amount into palm of hand. Rub together until dry.

OTHER INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified Water, Glycerin, Carbomer, Triethanolamine, Aloe Vera Oil, Aloe Vera Gel, Tocopherol Acetate

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Joelson_Hand Sanitizer_16oz01b LBL_Joelson_Hand Sanitizer_16oz

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62172-11862172-118-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
1019e9d8-1539-515d-e063-6294a90af86ca7e86ca4-669c-4cd3-b080-85e610b87cdf2024-01-29WarningsExact identifier
spl set id: a7e86ca4-669c-4cd3-b080-85e610b87cdf

Reported adverse events (FAERS/openFDA)#

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