FDA.reportPublic FDA data

74743-017 MOISTURIZING ANTIBACTERIAL HAND SANITIZER GEL

Manufacturer
Guangzhou Joy Claire Biological Technology Co.,Ltd
Effective date
2020-12-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:34:36

Label at a glance#

ProductMOISTURIZING ANTIBACTERIAL HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Dosage and administration

Open the cap and gently squeeze product into palm of hands, then rub throughly over all surfaces of both hands.

Storage and handling

Store between 59-86F(15-30C). Avoid freezing and excessive heat above 104F (40C).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on skin

Warnings

WARNINGS SECTION

For external use only, Keep out of reach of children.

Do not use

OTC - DO NOT USE SECTION

do not use in or near the eyes. In case of contaot, rinse eyes thoroughly with water.

OTC - WHEN USING SECTION

When using this product,
do not use in or near the eyes. In case of contaot, rinse eyes thoroughly with water.
Stop use and ask doctor if imtation or rash appears and lasts.
Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

OTC - STOP USE SECTION

Stop use and ask doctor if imtation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach for children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Open the cap and gently squeeze product into palm of hands, then rub throughly over all surfaces of both hands.

Other information

STORAGE AND HANDLING SECTION

Store between 59-86F(15-30C). Avoid freezing and excessive heat above 104F (40C).

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER (AQUA).
FRAGRANCE (PARFUM), PHENOXYETHANOL,
POLYQUATERNIUM-10, POLYSORBATE 20,
TETRASODIUM EDTA.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

74743-017-01 50ML74743-017-01 50ML

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1098199benzalkonium chloride 0.13 % Topical GelPSN1
1098199benzalkonium chloride 0.0013 MG/MG Topical GelSCD1
1098199benzalkonium chloride 0.13 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74743-017-012022-01-28C16284748780-1d6a99b39-99b8-a426-e053-dadaa90af4c274743-017 MOISTURIZING ANTIBACTERIAL HAND SANITIZER GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74743-017-01MOISTURIZING ANTIBACTERIAL HAND SANITIZER50 mL in 1 BOTTLEGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74743-017MOISTURIZING ANTIBACTERIAL HAND SANITIZER (MOISTURIZING ANTIBACTERIAL HAND SANITIZER GEL) GEL [GUANGZHOU JOY CLAIRE BIOLOGICAL TECHNOLOGY CO.,LTD]1Legacy NDC, 1 package rows20201204_b59ba2b0-5064-dbff-e053-2a95a90aebb0.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74743-01774743-017-01

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
POLYSORBATE 207T1F30V5YHIACT
EDETATE SODIUMMP1J8420LUIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
b59b951a-e0a7-0d8b-e053-2995a90aac04b59ba2b0-5064-dbff-e053-2a95a90aebb02020-12-03WarningsExact identifier
spl id: b59b951a-e0a7-0d8b-e053-2995a90aac04
spl set id: b59ba2b0-5064-dbff-e053-2a95a90aebb0