SPA SENSE Antibacterial Hand Wash-Lavender

Manufacturer: LAB-CLEAN, INC
Effective date: 2022-04-26
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:02:35

Label at a glance#

ProductSPA SENSE Antibacterial Hand Wash-Lavender

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Dosage and administration

Apply small amount of product to wet hands. Work into lather and rinse thorughly. Dry hands.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13 %

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

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

Stop use and ask a doctor if irritation or redness develops and condition persists.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply small amount of product to wet hands. Work into lather and rinse thorughly. Dry hands.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera, Benzisothiazol, Caprylyl Glucoside, Citric acid, Cocamide MIPA, Cocamidopropyl Betaine, Fragrance, Glycerine, Methylisathiozol, PEG-150 Distearate, Tetrasodium EDTA, Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

SPA SENSE Antibacterial Hand Wash-Lavender
BENZALKONIUM CHLORIDE
WATER
COCAMIDOPROPYL BETAINE
PEG-150 DISTEARATE
CAPRYLYL GLUCOSIDE
GLYCERIN
COCO MONOISOPROPANOLAMIDE
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
ALOE VERA LEAF
BENZISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73126-025	73126-025-01, 73126-025-02, 73126-025-03, 73126-025-04, 73126-025-05, 73126-025-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
PEG-150 DISTEARATE	6F36Q0I0AC	IACT
CAPRYLYL GLUCOSIDE	V109WUT6RL	IACT
GLYCERIN	PDC6A3C0OX	IACT
COCO MONOISOPROPANOLAMIDE	21X4Y0VTB1	IACT
EDETATE SODIUM	MP1J8420LU	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
BENZISOTHIAZOLINONE	HRA0F1A4R3	IACT
METHYLISOTHIAZOLINONE	229D0E1QFA	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
dd942843-3c78-475b-e053-2995a90a6872			f366534f-65ee-4085-a0b3-4a2b8ff37677	2022-04-26	Warnings	Exact identifier spl id: dd942843-3c78-475b-e053-2995a90a6872 spl set id: f366534f-65ee-4085-a0b3-4a2b8ff37677

Reported adverse events (FAERS/openFDA)#

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