FDA.reportPublic FDA data

LUCKY SUPER SOFT ANTIBACTERIAL HAND

Manufacturer
NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.
Effective date
2024-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:19:29

Label at a glance#

ProductLUCKY SUPER SOFT ANTIBACTERIAL HAND
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

wet hands and apply soap. lather all surfaces of hands and fingers by rubbing vigorously for at leat 20 seconds. rinse hands well and dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13 percent

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwahing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes, in case of eye contact, flush with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops, condition persists for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands and apply soap.

lather all surfaces of hands and fingers by rubbing vigorously for at leat 20 seconds.

rinse hands well and dry.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, PEG-150 distearate, sodium lauroamphoacetate, PEG-40 hydrogenated castor oil, fragrance, methylchloroisothiazolinone, methylisothiazolinone, citric acid, FD&C yellow no.5, FD&C red no.40

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

printingprinting

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76176-024-01LUCKY SUPER SOFT ANTIBACTERIAL HAND333 mL in 1 BOTTLE, PUMPLIQUID3331

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76176-024LUCKY SUPER SOFT ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) LIQUID [NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.]11 package rows20240915_215bb9c7-2177-d87b-e063-6394a90a41b0.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-02476176-024-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM LAUROAMPHOACETATESLK428451LIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
FD&C YELLOW NO. 5I753WB2F1MIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
FD&C RED NO. 40WZB9127XOAIACT

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
215bbd72-ee01-44a6-e063-6294a90a1972215bb9c7-2177-d87b-e063-6394a90a41b02024-01-01WarningsExact identifier
spl id: 215bbd72-ee01-44a6-e063-6294a90a1972
spl set id: 215bb9c7-2177-d87b-e063-6394a90a41b0

Reported adverse events (FAERS/openFDA)#

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