FDA.reportPublic FDA data

DMC NEAT HAND SANITIZING GEL (62172-115)

Manufacturer
DIVERSIFIED MANUFACTURING CORP
Effective date
2022-01-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:13:16

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

HAND SANITIZER TO DECREASE BACTERIA ON THE SKIN THAT CAUSES DISEASE. RECOMMENDED FOR REPEATED USE.

Dosage and administration

WET HANDS THOROUGHLY WITH THE PRODUCT AND ALLOW IT TO DRY WITHOUT WIPING. CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT. NOT RECOMMENDED FOR INFANTS.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 62%

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USES

INDICATIONS & USAGE SECTION

HAND SANITIZER TO DECREASE BACTERIA ON THE SKIN THAT CAUSES DISEASE. RECOMMENDED FOR REPEATED USE.

WARNINGS

WARNINGS SECTION

FOR EXTERNAL USE ONLY-HANDS.

FLAMMABLE. KEEP AWAY FROM HEAT AND FLAME.

WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IN CASE OF CONTACT, FLUSH EYES THOROUGHLY WITH WATER.

DO NOT INHALE OR INGEST. AVOID CONTACT WITH BROKEN SKIN.

STOP USE AND ASK A DOCTOR IF IRRITATION OR REDNESS DEVELOPS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

WET HANDS THOROUGHLY WITH THE PRODUCT AND ALLOW IT TO DRY WITHOUT WIPING. CHILDREN UNDER 6 YEARS OF AGE SHOULD BE SUPERVISED WHEN USING THIS PRODUCT.

NOT RECOMMENDED FOR INFANTS.

OTHER INFORMATION

OTHER SAFETY INFORMATION

DO NOT STORE ABOVE 104°F (40°C).

MAY DISCOLOR CERTAIN FABRICS OR SURFACES.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

PURIFIED WATER, GLYCERIN, CARBOMER, TRIETHANOLAMINE, ALOE VERA GEL, ALOE VERA OIL, TOCOPHERYL ACETATE, FRAGRANCE.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Neat_Hand Sanitizing Gel_3oz01b LBL_Neat_Hand Sanitizing Gel_3oz

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
62172-11562172-115-13

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
TROLAMINE9O3K93S3TKIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
1019a49e-8ede-5140-e063-6394a90ae12599cc10f9-a300-475e-adec-e4f33230271e2024-01-29WarningsExact identifier
spl set id: 99cc10f9-a300-475e-adec-e4f33230271e

Reported adverse events (FAERS/openFDA)#

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