HAND SANITIZER

Manufacturer
Detergent Marketing Systems, Inc.
Effective date
2020-05-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:16:26

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

OTC - PURPOSE SECTION

Uses: Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

WARNINGS SECTION

Warnings: For external use only. Flammable. Keep away from heat and flame.

OTC - WHEN USING SECTION

When using this product:

  • Do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
  • Avoid contact with broken skin.
  • Stop use and ask a doctor if skin irritation develops.

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.

DOSAGE & ADMINISTRATION SECTION

Directions: Wet hands thoroughly with product and allow to dry without wiping

  • For children under 6 years old, use only under adult supervision.
  • Not recommended for infants.

INDICATIONS & USAGE SECTION

Other Information:

  • Do not store above 105 degree F
  • May discolor some fabrics
  • Harmful to wood finishes and plastics.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: aloe vera, carbomer, glycerin, propylene glycol, water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sample labelsample label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73803-909-412022-01-28C16284748780-1d6a99b39-f30f-a426-e053-dadaa90af4c2a0fcbdea-9a01-37d5-e053-2995a90ab8cd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73803-909-41HAND SANITIZER3.78 L in 1 BOTTLE, PLASTICLIQUID3.781

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73803-909HAND SANITIZER (ETHYL ALCOHOL) LIQUID [DETERGENT MARKETING SYSTEMS, INC.]1Legacy NDC, 1 package rows20200608_a0fcbdea-9a01-37d5-e053-2995a90ab8cd.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
73803-90973803-909-41

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
a6155b5c-4dfc-1f43-e053-2a95a90a740ba0fcbdea-9a01-37d5-e053-2995a90ab8cd2020-05-18WarningsExact identifier
spl id: a6155b5c-4dfc-1f43-e053-2a95a90a740b
spl set id: a0fcbdea-9a01-37d5-e053-2995a90ab8cd

Reported adverse events (FAERS/openFDA)#

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