FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
In Designs Global LLC
Effective date
2023-10-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:57:47

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure8 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 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

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

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
  • In case of deep or punture wounds or serious burns, consult physician.
  • If redness, irritation, swelling, or pain persists or increases or if infection occurs discontinue use and physician.

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

Aminomethyl Propanol, Carbomer, Water. 

Questions?

OTC - QUESTIONS SECTION

  • 1-800-369-4670

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74712-000-01Hand Sanitizer50 mL in 1 BOTTLEGEL502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74712-000HAND SANITIZER (ALCOHOL) GEL [IN DESIGNS GLOBAL LLC]2Current NDC, Legacy NDC, 1 package rows20231026_a2dcedcd-e071-176e-e053-2a95a90a176b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74712-00074712-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYLPROPANOLLU49E6626QIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
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 SanitizerALCOHOLIn Designs Global LLCa2dcedcd-e071-176e-e053-2a95a90a176b2023-10-25WarningsExact identifier
ndc (package): 74712-000-01
ndc (product): 74712-000
ndc11 (package): 74712000001
spl id: 08966536-82bc-2006-e063-6294a90a243c
spl set id: a2dcedcd-e071-176e-e053-2a95a90a176b

Reported adverse events (FAERS/openFDA)#

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