FDA.reportPublic FDA data

Blue Devil Hand Sanitizer

Manufacturer
Blue Cross Laboratories | Ningbo Liyuan Daily Chemical Products Co., Ltd
Effective date
2020-05-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:30:19

Label at a glance#

ProductBlue Devil Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping. for children under 6, use only under adult supervision not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Uses

  • to decrease bacteria on the skin
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only-hands. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

  • not recommended for infants

INDICATIONS & USAGE SECTION

  • avoid contact with broken skin
  • do not inhale or ingest

OTC - WHEN USING SECTION

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.


Stop use and ask a doctor if

  • skin irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet hands thoroughly with product and allow to dry without wiping.
  • for children under 6, use only under adult supervision
  • not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, propylene glycol, carbomer

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Blue Devil

Hand Sanitizer

Fights 99.99% of germs and bacteria

Helps stop the spread of illness

Great for travel, home, & workplace

8oz. 237ml part #00245

419245419245

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
22431-22222431-222-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
a5b1f54a-a61f-d302-e053-2a95a90a2861a5b1f54a-a62d-d302-e053-2a95a90a28612020-05-15WarningsExact identifier
spl id: a5b1f54a-a61f-d302-e053-2a95a90a2861
spl set id: a5b1f54a-a62d-d302-e053-2a95a90a2861

Reported adverse events (FAERS/openFDA)#

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