Aoliben ZHUSHI hand sanitizer gel

Manufacturer
Shandong Zhushi Pharmaceutical Group Co., Ltd
Effective date
2022-03-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:48:41

Label at a glance#

ProductAoliben ZHUSHI hand sanitizer gel
Active ingredientALCOHOL, PROPYL ALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Protect from light, airtight, and moisture. Store in a cool, dry place.

INACTIVE INGREDIENT SECTION

Carbomer 980

Triethanolamine

Purified water

INDICATIONS & USAGE SECTION

1.Sanitary hand :Take a minute to take an appropriate amount of hand sanitizer on the palm of your hand, rub your hands together to coat each part evenly
2.Surgical hand :After surgical hand washing, take 3-5 minutes to take an appropriate amount of hand disinfectant and evenly apply it to the skin of the hands, forearms and lower thirds of the upper arms.

OTC - ACTIVE INGREDIENT SECTION

Alcohol

N-propanol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Topical disinfectants should not be taken orally and should be kept out of reach of children.

OTC - PURPOSE SECTION

Disinfection
Sterilization

WARNINGS SECTION

Flammable, keep away from fire.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56040-007-01Aoliben ZHUSHI hand sanitizer gel1000 mL in 1 BOTTLEGEL10004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56040-007AOLIBEN ZHUSHI HAND SANITIZER GEL (AOLIBEN ZHUSHI HAND SANITIZERGEL) GEL [SHANDONG ZHUSHI PHARMACEUTICAL GROUP CO., LTD]4Legacy NDC, 1 package rows20220311_af4172ac-da3e-4207-e053-2a95a90a54f2.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56040-00756040-007-01

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
d9db32be-0516-524e-e053-2995a90ac1fcaf4172ac-da3e-4207-e053-2a95a90a54f22022-03-10WarningsExact identifier
spl id: d9db32be-0516-524e-e053-2995a90ac1fc
spl set id: af4172ac-da3e-4207-e053-2a95a90a54f2

Reported adverse events (FAERS/openFDA)#

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