75% ALCOHOL DISNFECTANT

Manufacturer
ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD
Effective date
2024-04-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:05:07

Label at a glance#

Product75% ALCOHOL DISNFECTANT
Active ingredientALCOHOL
Label structure11 sections

Indications and uses

to decrease bacteria on the skin that could cause disease recommended for repeated use.

Dosage and administration

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.

Storage and handling

Do not store above 105ºF May discolor some fabrics Harmful to wood finishes and piastics.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 77%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

to decrease bacteria on the skin that could cause disease

recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only

Flammable

Keep away from fire or flame

OTC - WHEN USING SECTION

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

irritation or redness develops

condition persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical heip or contact a Poison Control Center right away.

Directions

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

Do not store above 105ºF

May discolor some fabrics

Harmful to wood finishes and piastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

20mL NDC: 73905-030-01 20ml20ml

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73905-03073905-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
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
165f0501-0403-b64b-e063-6394a90a76aab31da5ef-bdca-a1a8-e053-2a95a90a06fd2024-04-18WarningsExact identifier
spl id: 165f0501-0403-b64b-e063-6394a90a76aa
spl set id: b31da5ef-bdca-a1a8-e053-2a95a90a06fd

Reported adverse events (FAERS/openFDA)#

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