Antibacterial Hand gel

Manufacturer
Foshan MUZAR Cosmetics Co., Ltd
Effective date
2020-03-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:49

Label at a glance#

ProductAntibacterial Hand gel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Hand Sanitizer to help reduce bacteria on skin.

Dosage and administration

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry. Children under 6 years of age should be supervised when using this product.

Storage and handling

Store below 106° F.(41 ° C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 50%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.Stop use and ask doctor if irritation or rash appears and lasts.Keep out of reach for children. if swallowed,get medical help or contact a With Vitamin E& Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough Product in your palm to thoroughly spread on both hands and rub into the skin until dry.

Children under 6 years of age should be supervised when using this product.

Other information

STORAGE AND HANDLING SECTION

Store below 106° F.(41 ° C)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water,glycerin,cabo,alcohol,triethanolamine,940

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 mL label50 mL label100 mL label100 mL label200 mL label200 mL label300 mL label300 mL label500 mL label500 mL label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2287161ethanol 50 % Topical GelPSN1
2287161ethanol 0.5 ML/ML Topical GelSCD1
2287161ethanol 50 % Topical GelSY1
2287161ethyl alcohol 50 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74041-001-01Antibacterial Hand gel50 mL in 1 BOTTLEGEL501
74041-001-02Antibacterial Hand gel100 mL in 1 BOTTLEGEL1001
74041-001-03Antibacterial Hand gel200 mL in 1 BOTTLEGEL2001
74041-001-04Antibacterial Hand gel300 mL in 1 BOTTLEGEL3001
74041-001-05Antibacterial Hand gel500 mL in 1 BOTTLEGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74041-001ANTIBACTERIAL HAND GEL (ALCOHOL) GEL [FOSHAN MUZAR COSMETICS CO., LTD]1Legacy NDC, 5 package rows20200403_a227b16b-06e2-d741-e053-2a95a90a4a0a.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74041-00174041-001-01, 74041-001-02, 74041-001-03, 74041-001-04, 74041-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
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
a227b825-65c5-4c17-e053-2995a90af292a227b16b-06e2-d741-e053-2a95a90a4a0a2020-03-31WarningsExact identifier
spl id: a227b825-65c5-4c17-e053-2995a90af292
spl set id: a227b16b-06e2-d741-e053-2a95a90a4a0a

Reported adverse events (FAERS/openFDA)#

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