Hand Sanitizer

Manufacturer
NPW-USA, Inc.
Effective date
2016-01-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:45:00

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Storage and handling

Other Information: Do not store in temperatures above 118 F

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient:
Ethyl alcohol, 62%

OTC - PURPOSE SECTION

Purpose Antiseptic

WARNINGS SECTION

Warnings:

For external use only.

FLAMMBLE. Keep away from fire or flame.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation and redness persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Apply a small amount into palm of hand
  • Rub thoroughly over both hands until dry
  • Not to be rinsed off with water
  • Children must be supervised when using this product
  • For personal / domestic use
  • Do not dilute product

INACTIVE INGREDIENT SECTION

Inactive ingredients: water, glycerin, propylene glycol, fragrance, carbomer, triethanolamine, acrylates copolymer, polyethylene terephthalate, red 33, diatomaceous earth.

STORAGE AND HANDLING SECTION

Other Information:

Do not store in temperatures above 118 F

INDICATIONS & USAGE SECTION

Uses:

  • Hand sanitizer to help reduce bacteria on the skin.
  • Recommended for repeated use.

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of bottle labelimage of bottle label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49435-001-012023-01-30C16284748780-1f386c64a-2497-0266-e053-dadaa90a7c1a290f5411-fda2-6521-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49435-001-01Hand Sanitizer30 mL in 1 BOTTLE, SPRAYGEL301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49435-001HAND SANITIZER (ETHYL ALCOHOL) GEL [NPW-USA, INC.]1Legacy NDC, 1 package rows20160217_290f5411-fda2-6521-e054-00144ff88e88.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
49435-00149435-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
290f5411-fda4-6521-e054-00144ff88e88290f5411-fda2-6521-e054-00144ff88e882016-01-11WarningsExact identifier
spl id: 290f5411-fda4-6521-e054-00144ff88e88
spl set id: 290f5411-fda2-6521-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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