FDA.reportPublic FDA data

Lucky

Manufacturer
Delta Brands Inc.
Effective date
2020-12-14
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 23:01:54

Label at a glance#

ProductLucky antibacterial deodorant
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

■ for washing to decrease bacteria on the skin

Dosage and administration

■ wet bar with water ■ lather vigorously and wash skin ■ rinse and dry thoroughly

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 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 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

■ wet bar with water ■ lather vigorously and wash skin ■ rinse and dry thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

sodium palm kernelate, sodium palmate, water, fragrance, glycerin, sodium chloride, tetrasodium EDTA, FD&C yellow no. 5, FD&C red no. 4

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Stop use and ask a doctor if

OTC - STOP USE SECTION

■irritation and redness develops

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
20276-049-022020-12-14C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-302020-12-14C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-352020-12-14C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-022020-09-27C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-302020-09-27C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-352020-09-27C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-022020-09-25C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-302020-09-25C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-352020-09-25C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-022020-07-22C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-302020-07-22C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013
20276-049-352020-07-22C16284748780-1ab0e2407-28d8-f274-e053-dbdaa90a6471DltaAntibacSoapBKC013

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
20276-04920276-049-30, 20276-049-35, 20276-049-85, 20276-049-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM PALM KERNELATE6H91L1NXTWIACT
SODIUM PALMITATEJQ43KP6296IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SODIUM CHLORIDE451W47IQ8XIACT
EDETATE SODIUMMP1J8420LUIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C RED NO. 4X3W0AM1JLXIACT
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
b674745a-ef24-56ed-e053-2995a90ad0f2441efdff-8c5c-18e1-e054-00144ff8d46c2020-12-14WarningsExact identifier
spl id: b674745a-ef24-56ed-e053-2995a90ad0f2
spl set id: 441efdff-8c5c-18e1-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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