FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Gordon Industries | Bath Concept Cosmetics (Dongguan) Co., Ltd
Effective date
2023-10-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:57:55

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 water.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hanwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable, keep away from fire and flame

Does not 

OTC - DO NOT USE SECTION

contain grain alcohol; do not drink. if taken internally will produce serious gastric disturbance.

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 Contorl 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: (74640-010-30)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling: (74640-010-50)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74640-010-30Hand Sanitizer30 mL in 1 BOTTLEGEL302
74640-010-50Hand Sanitizer50 mL in 1 BOTTLEGEL502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74640-010HAND SANITIZER (ALCOHOL) GEL [GORDON INDUSTRIES]2Current NDC, Legacy NDC, 2 package rows20231026_e4846d7b-767b-41dd-ab49-dfc3d851f3e6.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
74640-01074640-010-30, 74640-010-50

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 · 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
Hand SanitizerALCOHOLGordon Industriese4846d7b-767b-41dd-ab49-dfc3d851f3e62023-10-25WarningsExact identifier
ndc (package): 74640-010-50
ndc (package): 74640-010-30
ndc (product): 74640-010
ndc11 (package): 74640001050
ndc11 (package): 74640001030
spl id: 0896e861-a79a-2dd8-e063-6294a90aaa3c
spl set id: e4846d7b-767b-41dd-ab49-dfc3d851f3e6

Reported adverse events (FAERS/openFDA)#

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