FDA.reportPublic FDA data

DERMA-GLOVE SPRAY

Manufacturer
RWM TECHNOLOGIES
Effective date
2010-06-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:25:14

Label at a glance#

ProductDerma-Glove
Active ingredientEthanol, Triclosan
Label structure10 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION


DERMA-GLOVE(R) hand sanitizer spray

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethanol 60%..................................................................Antibacterial

Triclosan 0.3% ..............................................................Antiseptic

OTC - PURPOSE SECTION

Antiseptic/Antimicrobial hand sanitizer spray

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease
  • Recommended for repeated use

WARNINGS AND PRECAUTIONS SECTION

Warnings

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product do not use in or near eyes. In case of eye contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness develops and persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the Reach of Children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:
  • Spray enough product in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Rinse with water after use
  • Children under 6 years of age should be supervised when using this product

GENERAL PRECAUTIONS SECTION

  • Do not store above 110o F (43o C)
  • For additional information, see Material Safety Data Sheet (MSDS).

INACTIVE INGREDIENT SECTION

Deionized Water, Glycereth-18 Ethylhexanoate, Glycereth-18, Polyoxyethylene (20) Sorbitan Monooleate, 2-Amino-2-methyl-1-propanol, Polyquaternium-69, Citric Acid and Sodium Citrate

OTC - QUESTIONS SECTION

Questions or Comments?

Call 1-888-300-1225 Monday through Friday 8:00 AM to 5:00 PM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LABEL FILELABEL FILELABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039706ethanol 62 % / triclosan 0.3 % Topical SprayPSN4
1039706ethanol 0.62 ML/ML / triclosan 3 MG/ML Topical SpraySCD4
1039706ethanol 62 % / triclosan 0.3 % Topical SpraySY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
24673-249-012019-10-21C16284748780-1956f9ecf-de5a-621f-e053-dbdaa90a74adDERMA-GLOVE SPRAY
24673-249-022019-10-21C16284748780-1956f9ecf-de5a-621f-e053-dbdaa90a74adDERMA-GLOVE SPRAY
24673-249-032019-10-21C16284748780-1956f9ecf-de5a-621f-e053-dbdaa90a74adDERMA-GLOVE SPRAY
24673-249-042019-10-21C16284748780-1956f9ecf-de5a-621f-e053-dbdaa90a74adDERMA-GLOVE SPRAY
24673-249-052019-10-21C16284748780-1956f9ecf-de5a-621f-e053-dbdaa90a74adDERMA-GLOVE SPRAY
24673-249-062019-10-21C16284748780-1956f9ecf-de5a-621f-e053-dbdaa90a74adDERMA-GLOVE SPRAY

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
24673-249-01Derma-Glove13.65 g in 1 BOTTLE, SPRAYSPRAY13.654
24673-249-02Derma-Glove3494.4 g in 1 BOTTLE, SPRAYSPRAY3494.44
24673-249-03Derma-Glove17472 g in 1 DRUMSPRAY174724
24673-249-04Derma-Glove192192 g in 1 DRUMSPRAY1921924
24673-249-05Derma-Glove873600 g in 1 DRUMSPRAY8736004
24673-249-06Derma-Glove1223040 g in 1 DRUMSPRAY12230404

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
24673-249DERMA-GLOVE (ETHANOL, TRICLOSAN) SPRAY [RWM TECHNOLOGIES]4Legacy NDC, 6 package rows20100715_f4f2115e-18bd-4cd2-8698-37d796c1588b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EthanolACTIVE INGREDIENT3K9958V90M4
TriclosanACTIVE INGREDIENT4NM5039Y5X4
EthanolACTIVE MOIETY3K9958V90M4
TriclosanACTIVE MOIETY4NM5039Y5X4

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
24673-24924673-249-01, 24673-249-02, 24673-249-03, 24673-249-04, 24673-249-05, 24673-249-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Ethanol3K9958V90MACTIB
Triclosan4NM5039Y5XACTIB

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
d3894ea4-022f-41b4-b1d2-59e0fcaef923f4f2115e-18bd-4cd2-8698-37d796c1588b2010-06-01WarningsExact identifier
spl id: d3894ea4-022f-41b4-b1d2-59e0fcaef923
spl set id: f4f2115e-18bd-4cd2-8698-37d796c1588b

Reported adverse events (FAERS/openFDA)#

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