Kitchen Lemon Zest Antibacterial Foaming Hand

Manufacturer: Apollo Health and Beauty Care Inc.
Effective date: 2019-08-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:00:07

Label at a glance#

ProductKitchen Lemon Zest Antibacterial Foaming Hand

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Indications and uses

for washing to decrease bacteria on the skin.

Dosage and administration

apply onto dry hands lather and rinse thoroughly

Storage and handling

store at room temperature

Contacts and useful links#

PhoneLabel contact1-866-695-3030

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 contact, rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation ad redness develops and lasts.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestiong, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

apply onto dry hands
lather and rinse thoroughly

Other information

STORAGE AND HANDLING SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Glycerin, Hydroxyethylcellulose, Polyquaternium-7, Benzophenone-4, Tetrasodium EDTA, Fragrance (Parfum), Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone, Yellow 5 (CI 19140), Red 40 (CI 16035).

Questions or comments?

OTC - QUESTIONS SECTION

1-866-695-3030

Label copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of the label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	1
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	1
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	1
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63148-016-12	2021-01-29	C162847	48780-1	ba0f9c33-32fd-a910-e053-dadaa90a0b85	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63148-016-12	Kitchen Lemon Zest Antibacterial Foaming Hand	355 mL in 1 BOTTLE, PLASTIC	SOAP	355		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63148-016	KITCHEN LEMON ZEST ANTIBACTERIAL FOAMING HAND (BENZALKONIUM CHLORIDE) SOAP [APOLLO HEALTH AND BEAUTY CARE INC.]	1	Legacy NDC, 1 package rows	20190822_2bf01fcc-04ba-4e20-b70a-bc3906d5d781.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Kitchen Lemon Zest Antibacterial Foaming Hand
Benzalkonium Chloride
BENZALKONIUM
WATER
COCAMIDOPROPYL BETAINE
GLYCERIN
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)
SULISOBENZONE
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C YELLOW NO. 5
FD&C RED NO. 40

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63148-016	63148-016-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
GLYCERIN	PDC6A3C0OX	IACT
HYDROXYETHYL CELLULOSE (5000 CPS AT 1%)	X70SE62ZAR	IACT
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)	0L414VCS5Y	IACT
SULISOBENZONE	1W6L629B4K	IACT
EDETATE SODIUM	MP1J8420LU	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C RED NO. 40	WZB9127XOA	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
e83e098d-84ed-45a4-b309-a7dd7faeaaa0			2bf01fcc-04ba-4e20-b70a-bc3906d5d781	2019-08-21	Warnings	Exact identifier spl id: e83e098d-84ed-45a4-b309-a7dd7faeaaa0 spl set id: 2bf01fcc-04ba-4e20-b70a-bc3906d5d781

Reported adverse events (FAERS/openFDA)#

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