BLUESEA INSTANT HAND SANITIZER

Manufacturer
BLUE SEA AEROSOL & DAILY CARE CO., LTD
Effective date
2024-12-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:41:11

Label at a glance#

ProductBLUESEA INSTANT HAND SANITIZER
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wet hands thoroughly with product and rub until dry without wiping For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Use anywhere without water

Warnings

WARNINGS SECTION

For external use only -hands

Flammable. Keep away from heat and flame

OTC - WHEN USING SECTION

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Avoid contact with broken skin

Do not inhale or ingest

OTC - STOP USE SECTION

Discontinue if skin becomes irritated and ask a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingest, seek professional assistance or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands thoroughly with product and rub until dry without wiping
  • For children under 6, use only under adult supervision
  • Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

Do not store above 105F

May discolor some fabrics

Harmful to wood finishes and plastics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, glycerin, carbomer, triethanolamine, Aloe

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN2
582753ethanol 0.7 ML/ML Topical SolutionSCD2
582753ethanol 70 % Topical SolutionSY2
582753ethyl alcohol 70 % Topical SolutionSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72119-003-01BLUESEA INSTANT HAND SANITIZER60 mL in 1 BOTTLESOLUTION602
72119-003-02BLUESEA INSTANT HAND SANITIZER100 mL in 1 BOTTLESOLUTION1002
72119-003-03BLUESEA INSTANT HAND SANITIZER237 mL in 1 BOTTLESOLUTION2372
72119-003-04BLUESEA INSTANT HAND SANITIZER300 mL in 1 BOTTLESOLUTION3002
72119-003-05BLUESEA INSTANT HAND SANITIZER500 mL in 1 BOTTLESOLUTION5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72119-003BLUESEA INSTANT HAND SANITIZER (ALCOHOL) SOLUTION [BLUE SEA AEROSOL & DAILY CARE CO., LTD]2Current NDC, Legacy NDC, 5 package rows20241208_e6b5ce49-d6d6-4b24-8b40-bfb1fb7005bd.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
72119-00372119-003-01, 72119-003-02, 72119-003-03, 72119-003-04, 72119-003-05

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
BLUESEA INSTANT HAND SANITIZERALCOHOLBLUE SEA AEROSOL & DAILY CARE CO., LTDe6b5ce49-d6d6-4b24-8b40-bfb1fb7005bd2024-12-06WarningsExact identifier
ndc (package): 72119-003-02
ndc (package): 72119-003-04
ndc (package): 72119-003-03
ndc (package): 72119-003-01
ndc (package): 72119-003-05
ndc (product): 72119-003
ndc11 (package): 72119000301
ndc11 (package): 72119000302
ndc11 (package): 72119000304
ndc11 (package): 72119000303
ndc11 (package): 72119000305
spl id: 289f17c4-dca7-a52e-e063-6394a90a41b0
spl set id: e6b5ce49-d6d6-4b24-8b40-bfb1fb7005bd

Reported adverse events (FAERS/openFDA)#

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