FDA.reportPublic FDA data

Clear Hand Sanitizing Gel

Manufacturer
Huizhou Bomei Cosmetic Co., Ltd.
Effective date
2021-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:24:54

Label at a glance#

ProductClear Hand Sanitizing
Active ingredientALCOHOL
Label structure7 sections

Dosage and administration

Rub into hands until dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Decreases bacteroa on hands

Warnings

WARNINGS SECTION

  • Flammable, keep away from heat or flame
  • For Extract Use Only

When using this product 

OTC - WHEN USING SECTION

keep out of eyes.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or redness develops.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Rub into hands until dry

Other information

SPL UNCLASSIFIED SECTION

Store below 105° F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glycerin, Carbomer, Propylene Glycol, Sodium Hydroxide, Parfum (Fragrance), Aloe Barbadensis Leaf Extract.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72505-03072505-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM HYDROXIDE55X04QC32IIACT
ALOE VERA LEAFZY81Z83H0XIACT
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
d2401713-519a-1005-e053-2a95a90af8c0b7370ea5-84c7-9a35-e053-2a95a90acca32021-12-03WarningsExact identifier
spl id: d2401713-519a-1005-e053-2a95a90af8c0
spl set id: b7370ea5-84c7-9a35-e053-2a95a90acca3

Reported adverse events (FAERS/openFDA)#

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