Antibacterial

Manufacturer: Brands International Corporation
Effective date: 2021-01-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:37:28

Label at a glance#

ProductAntibacterial Coconut Water Aloe and Vitamin E

Active ingredientBENZALKONIUM CHLORIDE

Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride - 0.13%

OTC - PURPOSE SECTION

Purpose - Antiseptic Skin cleanser

INDICATIONS & USAGE SECTION

Effective in destroying (harmful) bacteria to provide antiseptic cleansing

WARNINGS SECTION

Warnings For external use only

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops

OTC - WHEN USING SECTION

When using this product

avoid contact with eyes.
If contact occurs, rinse eye thoroughly with water

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children :

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

DOSAGE & ADMINISTRATION SECTION

Directions:

For occasional and personal domestic use
Supervise children when they use this product.
Lather in hands with water for at least 30 seconds.
Rinse well.

INACTIVE INGREDIENT SECTION

Lauramidopropylamine oxide, Lauryl Glucoside, PEG-150 distearate, Glycol Stearate, Perfume, PEG-7 glycerly cocoate, Cetrimonium Chloride, Citric Acid, Glycerin, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, Isopropyl myristate, Tocopheryl Acetate

OTHER SAFETY INFORMATION

Store below 59F-86F
May discolor certain fabrics or surfaces.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

9101112

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	2
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	2
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	2
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50157-516-10	2025-01-30	C162847	48780-1	2cef2736-af13-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap - Coconut water
50157-516-23	2025-01-30	C162847	48780-1	2cef2736-af13-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap - Coconut water
50157-516-37	2025-01-30	C162847	48780-1	2cef2736-af13-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap - Coconut water
50157-516-44	2025-01-30	C162847	48780-1	2cef2736-af13-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap - Coconut water

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
50157-516-10	AntibacterialCoconut Water Aloe and Vitamin E	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000	2
50157-516-23	AntibacterialCoconut Water Aloe and Vitamin E	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	2
50157-516-37	AntibacterialCoconut Water Aloe and Vitamin E	3780 mL in 1 BOTTLE, PLASTIC	LIQUID	3780	2
50157-516-44	AntibacterialCoconut Water Aloe and Vitamin E	443 mL in 1 BOTTLE, PLASTIC	LIQUID	443	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50157-516	ANTIBACTERIAL COCONUT WATER ALOE AND VITAMIN E (BENZALKONIUM CHLORIDE) LIQUID [BRANDS INTERNATIONAL CORPORATION]	2	Legacy NDC, 4 package rows	20210128_af70531b-b071-4dc3-8d29-b63e3b30457f.zip

Products#

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

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

Antibacterial Coconut Water Aloe and Vitamin E
Benzalkonium Chloride
CITRIC ACID MONOHYDRATE
WATER
CETRIMONIUM CHLORIDE
ISOPROPYL MYRISTATE
GLYCOL STEARATE
LAURAMIDOPROPYLAMINE OXIDE
PEG-7 GLYCERYL COCOATE
DITETRACYCLINE TETRASODIUM EDETATE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
.ALPHA.-TOCOPHEROL ACETATE
ALOE VERA LEAF
PEG-150 DISTEARATE
LAURYL GLUCOSIDE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50157-516	50157-516-37, 50157-516-10, 50157-516-23, 50157-516-44

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
Name	UNII	Kind
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
WATER	059QF0KO0R	IACT
CETRIMONIUM CHLORIDE	UC9PE95IBP	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
GLYCOL STEARATE	0324G66D0E	IACT
LAURAMIDOPROPYLAMINE OXIDE	I6KX160QTV	IACT
PEG-7 GLYCERYL COCOATE	VNX7251543	IACT
DITETRACYCLINE TETRASODIUM EDETATE	WX0A0IT7K5	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
PEG-150 DISTEARATE	6F36Q0I0AC	IACT
LAURYL GLUCOSIDE	76LN7P7UCU	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
b9e40c73-c2f6-faaa-e053-2a95a90a5c47			af70531b-b071-4dc3-8d29-b63e3b30457f	2021-01-27	Warnings	Exact identifier spl id: b9e40c73-c2f6-faaa-e053-2a95a90a5c47 spl set id: af70531b-b071-4dc3-8d29-b63e3b30457f

Reported adverse events (FAERS/openFDA)#

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