FDA.reportPublic FDA data

LABCCIN Sanitizer gel

Manufacturer
Doori Cosmetics Co., Ltd.
Effective date
2021-06-30
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 22:41:38

Label at a glance#

ProductLABCCIN Sanitizer gel
Active ingredientALCOHOL
Label structure8 sections

Storage and handling

Store below 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

  • Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

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.

Direction

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

  • Store below 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Carbomer, Aminomethyl Propanol, Fragrance, Glycerin, Paeonia Suffruticosa Root Extract, Camellia Sinensis Leaf Extract, Aloe Ferox Leaf Extract, CITRUS PARADISI (GRAPEFRUIT) FRUIT EXTRACT

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50375-00350375-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
GLYCERINPDC6A3C0OXIACT
PAEONIA X SUFFRUTICOSA ROOT7M7E9A2C8JIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
ALOE FEROX LEAF0D145J8EMEIACT
GRAPEFRUITO82C39RR8CIACT
ALCOHOL3K9958V90MACTIB

Source Document#

Source XML · Source PDF

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
cd27245a-9ea3-a682-e053-2a95a90af9fd4e29db0c-5108-4a4c-9ffa-34ea8d98571f2021-09-29WarningsExact identifier
spl set id: 4e29db0c-5108-4a4c-9ffa-34ea8d98571f

Reported adverse events (FAERS/openFDA)#

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