Hand Sanitizer

Manufacturer
K7 Design Group Inc.
Effective date
2020-04-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:07:26

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

■ wet hands thoroughly with product and allow to dry without wiping

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, only when water is not available

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

■ do not get into eyes ■ if contact occurs; rinse eyes thoroughly with water

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ irritation and redness develop

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, get medical help or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

■ Store below 105ºF ■ May discolor some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PEG-40 Hydrogenated Castor Oil, Fragrance, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
247835ethanol 62 % Topical SolutionPSN2
247835ethanol 0.62 ML/ML Topical SolutionSCD2
247835ethanol 62 % Topical SolutionSY2
247835ethyl alcohol 62 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74177-001-01Hand Sanitizer50 mL in 1 BOTTLE, PLASTICLIQUID502
74177-001-08Hand Sanitizer236 mL in 1 BOTTLE, PUMPLIQUID2362
74177-001-12Hand Sanitizer354 mL in 1 BOTTLE, PUMPLIQUID3542
74177-001-16Hand Sanitizer473 mL in 1 BOTTLE, PUMPLIQUID4732
74177-001-30Hand Sanitizer887 mL in 1 BOTTLE, PUMPLIQUID8872
74177-001-34Hand Sanitizer1000 mL in 1 BOTTLE, PUMPLIQUID10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74177-001HAND SANITIZER (ALCOHOL) LIQUID [K7 DESIGN GROUP INC.]2Legacy NDC, 6 package rows20200423_a2654ceb-367e-e795-e053-2995a90a756f.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
74177-00174177-001-01, 74177-001-08, 74177-001-16, 74177-001-12, 74177-001-30, 74177-001-34

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
a3e4bfcc-864d-5cd0-e053-2995a90a4804a2654ceb-367e-e795-e053-2995a90a756f2020-04-22WarningsExact identifier
spl id: a3e4bfcc-864d-5cd0-e053-2995a90a4804
spl set id: a2654ceb-367e-e795-e053-2995a90a756f

Reported adverse events (FAERS/openFDA)#

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