Antibacterial Moisturizing

Manufacturer: Brands International Corporation
Effective date: 2020-09-17
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:29:40

Label at a glance#

ProductAntibacterial Moisturizing 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

do not get it into 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

wet hands
apply palmful to hands
scrub thoroughly
rinse
For occasional and personal domestic use
Supervise children when they use this product.

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 110 F (43)
May discolor certain fabrics or surfaces.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1234

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
50157-509-10	2025-01-30	C162847	48780-1	2cef2736-934d-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap
50157-509-23	2025-01-30	C162847	48780-1	2cef2736-934d-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap
50157-509-37	2025-01-30	C162847	48780-1	2cef2736-934d-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap
50157-509-44	2025-01-30	C162847	48780-1	2cef2736-934d-d83d-e063-dadaa90ab31f	Germs be Gone Antibacterial Hand Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
50157-509-10	Antibacterial MoisturizingAloe and Vitamin E	1000 mL in 1 BOTTLE, PLASTIC	LIQUID	1000	1
50157-509-23	Antibacterial MoisturizingAloe and Vitamin E	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236	1
50157-509-37	Antibacterial MoisturizingAloe and Vitamin E	3780 mL in 1 BOTTLE, PLASTIC	LIQUID	3780	1
50157-509-44	Antibacterial MoisturizingAloe and Vitamin E	443 mL in 1 BOTTLE, PLASTIC	LIQUID	443	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50157-509	ANTIBACTERIAL MOISTURIZING ALOE AND VITAMIN E (BENZALKONIUM CHLORIDE) LIQUID [BRANDS INTERNATIONAL CORPORATION]	1	Legacy NDC, 4 package rows	20200918_af87156e-a460-9f09-e053-2a95a90adb3d.zip

Products#

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

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50157-509	50157-509-37, 50157-509-23, 50157-509-44, 50157-509-10

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
CITRIC ACID MONOHYDRATE	2968PHW8QP	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
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
PEG-150 DISTEARATE	6F36Q0I0AC	IACT
LAURYL GLUCOSIDE	76LN7P7UCU	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
af873fa4-b5c0-1872-e053-2995a90a70e0			af87156e-a460-9f09-e053-2a95a90adb3d	2020-09-17	Warnings	Exact identifier spl id: af873fa4-b5c0-1872-e053-2995a90a70e0 spl set id: af87156e-a460-9f09-e053-2a95a90adb3d

Reported adverse events (FAERS/openFDA)#

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