Antimicrobial Foaming Hand

Manufacturer: Health Technology Professional Products, Inc
Effective date: 2025-03-07
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:57:01

Label at a glance#

ProductAntimicrobial Foaming Hand

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Indications and uses

• For hand sanitizing to decrease bacteria on the skin • Recommended for repeated use

Dosage and administration

Apply small amount of product to wet hands • Work into lather and rinse thoroughly • Dry hands

Label contents#

Full prescribing information#

Active Ingredient (in each use)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride .13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria on the skin

• Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of contact flush eyes with water. Do not ingest,

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develop and condition persists.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply small amount of product to wet hands • Work into lather and rinse thoroughly • Dry hands

Inactive ingredinets

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Lead Juice, Caprylyl/Capryl Glucoside, Citric Acid, Cocamidopropyl Betaine, FD&C Red 340, FD&C Yellow #5, Fragrance, Glycerine, Lauryl Polyglucose, Magnesium Nitrate, Maltodextrin, Methylchloroisothiazolinone, Methylisothiazolinone, Tetrasodium EDTA, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sample

sample

16 oz

Pump

1 - Gallon

Gallon

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	PSN	3
1046593	benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap	SCD	3
1046593	benzalkonium chloride 0.13 % Medicated Liquid Soap	SY	3
1046593	benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
81775-100-01	2025-03-12	C162847	48780-1	1030e365-58eb-111a-e063-dadaa90a10e2	Health Technology - Antimicrobial Foaming Hand Soap
81775-100-02	2025-03-12	C162847	48780-1	1030e365-58eb-111a-e063-dadaa90a10e2	Health Technology - Antimicrobial Foaming Hand Soap
81775-100-03	2025-03-12	C162847	48780-1	1030e365-58eb-111a-e063-dadaa90a10e2	Health Technology - Antimicrobial Foaming Hand Soap
81775-100-01	2024-01-30	C162847	48780-1	1030e365-58eb-111a-e063-dadaa90a10e2	Health Technology - Antimicrobial Foaming Hand Soap
81775-100-02	2024-01-30	C162847	48780-1	1030e365-58eb-111a-e063-dadaa90a10e2	Health Technology - Antimicrobial Foaming Hand Soap
81775-100-03	2024-01-30	C162847	48780-1	1030e365-58eb-111a-e063-dadaa90a10e2	Health Technology - Antimicrobial Foaming Hand Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
81775-100-01	Antimicrobial Foaming Hand	50.28 mL in 1 BOTTLE, PUMP	SOAP	50.28	3
81775-100-02	Antimicrobial Foaming Hand	500 mL in 1 BOTTLE, PUMP	SOAP	500	3
81775-100-03	Antimicrobial Foaming Hand	3785.4 mL in 1 BOTTLE	SOAP	3785.4	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81775-100	ANTIMICROBIAL FOAMING HAND (BENZALKONIUM CHLORIDE) SOAP [HEALTH TECHNOLOGY PROFESSIONAL PRODUCTS, INC]	3	Current NDC, Legacy NDC, 3 package rows	20250313_dbca0970-88ca-04a4-e053-2995a90a68f2.zip

Products#

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

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

Antimicrobial Foaming Hand
Benzalkonium Chloride
MAGNESIUM NITRATE
BENZALKONIUM
GLYCERIN
EDETATE SODIUM
FD&C RED NO. 40
COCAMIDOPROPYL BETAINE
CITRIC ACID MONOHYDRATE
FD&C YELLOW NO. 5
ALOE VERA LEAF
WATER
CAPRYLYL GLUCOSIDE
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
MALTODEXTRIN
LAURYL GLUCOSIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
81775-100	81775-100-01, 81775-100-02, 81775-100-03

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
MAGNESIUM NITRATE	77CBG3UN78	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
GLYCERIN	PDC6A3C0OX	IACT
EDETATE SODIUM	MP1J8420LU	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
WATER	059QF0KO0R	IACT
CAPRYLYL GLUCOSIDE	V109WUT6RL	IACT
METHYLCHLOROISOTHIAZOLINONE	DEL7T5QRPN	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	IACT
MALTODEXTRIN	7CVR7L4A2D	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
Antimicrobial Foaming Hand	BENZALKONIUM CHLORIDE	Health Technology Professional Products, Inc	dbca0970-88ca-04a4-e053-2995a90a68f2	2025-03-07	Warnings	Exact identifier ndc (package): 81775-100-03 ndc (package): 81775-100-01 ndc (package): 81775-100-02 ndc (product): 81775-100 ndc11 (package): 81775010002 ndc11 (package): 81775010003 ndc11 (package): 81775010001 spl id: 2fbac9d4-5f01-0ce7-e063-6394a90a3573 spl set id: dbca0970-88ca-04a4-e053-2995a90a68f2

Reported adverse events (FAERS/openFDA)#

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