FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Robert Gordon Ind. Ltd.
Effective date
2024-02-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:08:28

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Rub dime sized amount between hands until dry. Supervise children in the use of this product. In the case of eye contact, rinse eyes thoroughly with water.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75 %

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

  • Flammable, keep away from fire and flame
  • Does not contain grain alcohol; do not drink if taken internally will produce serious gastric distric disturbances.

When using this product

OTC - WHEN USING SECTION

  • Avoid the eyes and mucous membranes
  • In the case of eyes or mucous membranes contact, rinse area thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Condition worsens
  • Redness or irritation develops
  • Condition persists for more than 3 days

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed,contact a doctor or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Rub dime sized amount between hands until dry.
  • Supervise children in the use of this product.
  • In the case of eye contact, rinse eyes thoroughly with water.

Other information

SPL UNCLASSIFIED SECTION

  • Store below 105 °F
  • May discolor some fabrics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol.

Questions?

OTC - QUESTIONS SECTION

  • 516-354-8888

Package Labeling: 100ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle2Bottle2

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle3Bottle3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047755ethanol 75 % Topical SolutionPSN3
1047755ethanol 0.75 ML/ML Topical SolutionSCD3
1047755ethanol 75 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74979-002-102025-07-29C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-252025-07-29C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-502025-07-29C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-102024-01-30C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-252024-01-30C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-502024-01-30C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-102023-02-13C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-252023-02-13C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-502023-02-13C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-102023-01-30C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-252023-01-30C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer
74979-002-502023-01-30C16284748780-1f386c649-f959-0266-e053-dadaa90a7c1aHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74979-002-10Hand Sanitizer100 mL in 1 BOTTLELIQUID1003
74979-002-25Hand Sanitizer250 mL in 1 BOTTLELIQUID2503
74979-002-50Hand Sanitizer500 mL in 1 BOTTLELIQUID5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74979-002HAND SANITIZER (ALCOHOL) LIQUID [ROBERT GORDON IND. LTD.]3Legacy NDC, 3 package rows20240210_7e2b3838-3e79-4256-91ea-70365f1acb25.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74979-00274979-002-10, 74979-002-25, 74979-002-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALCOHOL3K9958V90MACTIB

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
10f40497-0a40-0e47-e063-6294a90a2b627e2b3838-3e79-4256-91ea-70365f1acb252024-02-09WarningsExact identifier
spl id: 10f40497-0a40-0e47-e063-6294a90a2b62
spl set id: 7e2b3838-3e79-4256-91ea-70365f1acb25

Reported adverse events (FAERS/openFDA)#

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