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

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

LUCKY antibacterial
Benzalkonium chloride
WATER
COCAMIDOPROPYL BETAINE
COCO GLUCOSIDE
GLYCERYL OLEATE
GLYCERIN
CETRIMONIUM CHLORIDE
COCO MONOETHANOLAMIDE
PEG-150 DISTEARATE
SODIUM CHLORIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
CITRIC ACID MONOHYDRATE
FD&C BLUE NO. 1
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
20276-147	20276-147-12, 20276-147-75, 20276-147-09, 20276-147-11, 20276-147-14, 20276-147-15, 20276-147-16, 20276-147-40, 20276-147-64

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
COCO GLUCOSIDE	ICS790225B	IACT
GLYCERYL OLEATE	4PC054V79P	IACT
GLYCERIN	PDC6A3C0OX	IACT
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
COCO MONOETHANOLAMIDE	C80684146D	IACT
PEG-150 DISTEARATE	6F36Q0I0AC	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

Source Document#

Source XML · Source PDF

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
feba204b-205d-3120-e053-6394a90a82e7			3283c8d4-9cc8-5d50-e054-00144ff8d46c	2023-06-22	Warnings	Exact identifier spl id: feba204b-205d-3120-e053-6394a90a82e7 spl set id: 3283c8d4-9cc8-5d50-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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