FDA.reportPublic FDA data

77720-016 CLEANZE SANITIZING GEL 70% Ethyl Alcohol

Manufacturer
Skaffles Group Limited Liability Company | Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Effective date
2021-01-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:22

Label at a glance#

ProductCLEANZE HAND SANITIZING
Active ingredientALCOHOL
Label structure6 sections

Dosage and administration

Directions . Pump a small amount in your palm and briskly rub hands together until dry. Children under 6 years of age should be supervised when in use. Other information . Store between 15 and 30C(59 and 86F).· Avoid freezing and excessive heat above 40C(104F).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 71%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use.

Warning

WARNINGS SECTION

For external use only. Flammable. Keep away from fire or flame. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Discontinue use if irritation and redness develop. lf condition persists for more than 72 hours consult a physician.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions . Pump a small amount in your palm and briskly rub hands together until dry.
Children under 6 years of age should be supervised when in use. Other information . Store between 15 and 30C(59 and 86F).· Avoid freezing and excessive heat above 40C(104F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, Carbomer,Glycerin,Tocopheryl Acetate (Vitamin E), Triethanolamine, Water(Aqua).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130742797900131GTIN-13: 0742797900131
EAN-13: 0742797900131
GTIN-12: 742797900131
UPC-A: 742797900131
GTIN storage (14 digits): 00742797900131		141765f7-c8ee-47b7-b7ab-a09c18d7e9e7.jpg
BarcodeEAN-130742797920931GTIN-13: 0742797920931
EAN-13: 0742797920931
GTIN-12: 742797920931
UPC-A: 742797920931
GTIN storage (14 digits): 00742797920931		788bc2b8-7cf3-4c6f-9069-d274e36a42d9.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77720-016-012025-01-30C16284748780-12cef2736-6ed8-d83d-e063-dadaa90ab31f77720-016 CLEANZE SANITIZING GEL 70% Ethyl Alcohol
77720-016-022025-01-30C16284748780-12cef2736-6ed8-d83d-e063-dadaa90ab31f77720-016 CLEANZE SANITIZING GEL 70% Ethyl Alcohol
77720-016-032025-01-30C16284748780-12cef2736-6ed8-d83d-e063-dadaa90ab31f77720-016 CLEANZE SANITIZING GEL 70% Ethyl Alcohol
77720-016-042025-01-30C16284748780-12cef2736-6ed8-d83d-e063-dadaa90ab31f77720-016 CLEANZE SANITIZING GEL 70% Ethyl Alcohol
77720-016-052025-01-30C16284748780-12cef2736-6ed8-d83d-e063-dadaa90ab31f77720-016 CLEANZE SANITIZING GEL 70% Ethyl Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77720-016-01CLEANZE HAND SANITIZING500 mL in 1 BOTTLEGEL5001
77720-016-02CLEANZE HAND SANITIZING1000 mL in 1 BOTTLEGEL10001
77720-016-03CLEANZE HAND SANITIZING237 mL in 1 BOTTLEGEL2371
77720-016-04CLEANZE HAND SANITIZING60 mL in 1 BOTTLEGEL601
77720-016-05CLEANZE HAND SANITIZING100 mL in 1 BOTTLEGEL1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77720-016CLEANZE HAND SANITIZING (ETHYL ALCOHOL) GEL [SKAFFLES GROUP LIMITED LIABILITY COMPANY]1Legacy NDC, 5 package rows20210102_b7e2e993-05f3-e992-e053-2995a90aa188.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77720-01677720-016-01, 77720-016-04, 77720-016-03, 77720-016-05, 77720-016-02

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
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
TROLAMINE9O3K93S3TKIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT

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
b7e2e277-352f-edb9-e053-2995a90aaf2ab7e2e993-05f3-e992-e053-2995a90aa1882021-01-02WarningsExact identifier
spl id: b7e2e277-352f-edb9-e053-2995a90aaf2a
spl set id: b7e2e993-05f3-e992-e053-2995a90aa188

Reported adverse events (FAERS/openFDA)#

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