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 structure9 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 wtaer.

Storage and handling

Store below 105 o F May discolor some fabrics.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For hand washing 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 disturbances.

When using this product

OTC - WHEN USING SECTION

  • Avoid the eyes and mucous membranes
  •  In 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 wtaer.

​Other information

STORAGE AND HANDLING SECTION

  • Store below 105 oF
  • May discolor some fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Fragrance, Carbomer, Aminomethyl propanol, Microcrystalline Cellulose, Lactose, Corn Starch Modified, Jojoba Esters, Ultramarines, FD&C Yellow No. 5, FD&C Blue No. 1

​Questions?

OTC - QUESTIONS SECTION

  • 516-354-8888

Package Labeling: 30mL 74979-001-30

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30mL30mL

Package Labeling: 50mL 74979-001-50

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50mL50mL

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
74979-001-302025-07-29C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-502025-07-29C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-302024-01-30C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-502024-01-30C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-302023-02-13C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-502023-02-13C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-302023-01-30C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer
74979-001-502023-01-30C16284748780-1f386c649-f785-0266-e053-dadaa90a7c1aHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74979-001-30Hand Sanitizer30 mL in 1 BOTTLELIQUID303
74979-001-50Hand Sanitizer50 mL in 1 BOTTLELIQUID503

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74979-001HAND SANITIZER (ALCOHOL) LIQUID [ROBERT GORDON IND. LTD.]3Legacy NDC, 2 package rows20240210_da77d9a6-284c-43fe-b03f-d313b48cbafe.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74979-00174979-001-30, 74979-001-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
MICROCRYSTALLINE CELLULOSEOP1R32D61UIACT
LACTOSE, UNSPECIFIED FORMJ2B2A4N98GIACT
STARCH, CORNO8232NY3SJIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
10f377d3-4bf7-bda5-e063-6294a90af320da77d9a6-284c-43fe-b03f-d313b48cbafe2024-02-09WarningsExact identifier
spl id: 10f377d3-4bf7-bda5-e063-6294a90af320
spl set id: da77d9a6-284c-43fe-b03f-d313b48cbafe

Reported adverse events (FAERS/openFDA)#

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