75% Alcohol Rinse-free antibacterial gel

Manufacturer
Biocaro Pharmaceutical Co., Ltd
Effective date
2020-06-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:24:46

Label at a glance#

Product75% Alcohol Rinse-free antibacterial gel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Apply Appropriate This Gel On Your Hand, And Rub Without Washing.

Storage and handling

Sealed, protected from lightstored in a cool and dry placeI Shelf lifel 12 months

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 75% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

disinfection , Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Suitable For Cleaning AndDisinfecting Your Hand To AvoidMicroorganisms Breed, Such AsEscherichia Coli, Staphylococcus AureusCandida Albicans

Warnings

WARNINGS SECTION

Warning For External Use, Oral Administration Is Prohibited: Those Who Are Allergic To Ethanol Are Prohibited Stay Away From Fire Sources: Keep Out of Reach Of Children

Do not use

OTC - DO NOT USE SECTION

  • Those who are allergic to ethanol are prohibited, stay away from fire soureces

OTC - WHEN USING SECTION

use Suitable For Cleaning AndDisinfecting Your Hand To AvoidMicroorganisms Breed, Such As Escherichia Coli, Staphylococcus Aureus Candida Albicans

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply Appropriate This Gel On Your Hand, And Rub Without Washing.

Other information

STORAGE AND HANDLING SECTION

Sealed, protected from lightstored in a cool and dry placeI Shelf lifel 12 months

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, carbopol , glycerol, triethanoiamine, essence

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78872-00178872-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
c0d8b2be-481a-67d4-e053-2995a90af3daa83efd20-a20e-26f7-e053-2a95a90ab1452021-04-26WarningsExact identifier
spl set id: a83efd20-a20e-26f7-e053-2a95a90ab145

Reported adverse events (FAERS/openFDA)#

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