FDA.reportPublic FDA data

LUCKY

Manufacturer
Delta Brands, Inc
Effective date
2023-06-22
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:29:38

Label at a glance#

ProductLUCKY antibacterial
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

for hand washing to decrease bacteria on the skin

Dosage and administration

■ pump into hands, wet as needed ■ lather vigorously for at least 15 seconds ■ wash skin, rinse thoroughly and dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

for hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

■ avoid contact with the eyes. In case of eye contact, flush with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION


■ irritation and redness develops

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

■ pump into hands, wet as needed ■ lather vigorously for at least 15 seconds ■ wash skin, rinse thoroughly and dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, cetrimonium chloride, coco-glucoside, glyceryl oleate, cocamide MEA, glycerin, PEG-150 distearate, sodium chloride, fragrance, citric acid, methylchloroisothiazolinone, methylisothiazolinone, FDC blue no. 1, DC red no. 33

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-14420276-144-13, 20276-144-75, 20276-144-09, 20276-144-11, 20276-144-14, 20276-144-15, 20276-144-16, 20276-144-40, 20276-144-64

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCO GLUCOSIDEICS790225BIACT
GLYCERYL OLEATE4PC054V79PIACT
GLYCERINPDC6A3C0OXIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
COCO MONOETHANOLAMIDEC80684146DIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
D&C RED NO. 339DBA0SBB0LIACT

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
feba4ab4-4555-de12-e053-6394a90a4bc64af3508e-4c2c-44f0-e054-00144ff8d46c2023-06-22WarningsExact identifier
spl id: feba4ab4-4555-de12-e053-6394a90a4bc6
spl set id: 4af3508e-4c2c-44f0-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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