WhiskCare 387

Manufacturer: Whisk Products, Inc.
Effective date: 2025-03-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:01:23

Label at a glance#

ProductWhiskCare 387

Active ingredientBENZALKONIUM CHLORIDE

Label structure7 sections

Dosage and administration

Apply a palmful to hands and forearms. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Use

INDICATIONS & USAGE SECTION

reduces amount of bacteria on hands

Warnings

WARNINGS SECTION

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

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 a palmful to hands and forearms.
Scrub thoroughly for at least fifteen seconds.
Rinse completely and dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, DMDM Hydantoin, Citric Acid, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label - 1 Gallon Short Neck Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	PSN	1
1233282	benzalkonium chloride 1 MG/ML Medicated Liquid Soap	SCD	1
1233282	benzalkonium chloride 0.1 % Medicated Liquid Soap	SY	1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
65585-531-01	WhiskCare 387	50 mL in 1 BOTTLE, PUMP	SOLUTION	50	1
65585-531-03	WhiskCare 387	8 in 1 BOX	SOLUTION	8	1
65585-531-03	WhiskCare 387	1000 mL in 1 BAG	SOLUTION	1000	1
65585-531-04	WhiskCare 387	500 mL in 1 BOTTLE, PUMP	SOLUTION	500	1
65585-531-04	WhiskCare 387	6 in 1 BOX	SOLUTION	6	1
65585-531-06	WhiskCare 387	3785 mL in 1 BOTTLE, PLASTIC	SOLUTION	3785	1
65585-531-08	WhiskCare 387	4 in 1 BOX	SOLUTION	4	1
65585-531-08	WhiskCare 387	1000 mL in 1 BAG	SOLUTION	1000	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65585-531	WHISKCARE 387 (BENZALKONIUM CHLORIDE) SOLUTION [WHISK PRODUCTS, INC.]	1	Current NDC, 8 package rows	20250523_35bb7d59-111e-fa47-e063-6394a90aaf1e.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

WhiskCare 387
Benzalkonium Chloride
WATER
PEG-120 METHYL GLUCOSE DIOLEATE
GLYCERIN
LAURAMINE OXIDE
BENZALKONIUM
DMDM HYDANTOIN
CITRIC ACID MONOHYDRATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65585-531	65585-531-01, 65585-531-03, 65585-531-04, 65585-531-06, 65585-531-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PEG-120 METHYL GLUCOSE DIOLEATE	YM0K64F20V	IACT
GLYCERIN	PDC6A3C0OX	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
DMDM HYDANTOIN	BYR0546TOW	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	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
WhiskCare 387	BENZALKONIUM CHLORIDE	Whisk Products, Inc.	35bb7d59-111e-fa47-e063-6394a90aaf1e	2025-03-31	Warnings	Exact identifier ndc (package): 65585-531-06 ndc (package): 65585-531-03 ndc (package): 65585-531-08 ndc (package): 65585-531-04 ndc (package): 65585-531-01 ndc (product): 65585-531 ndc11 (package): 65585053106 ndc11 (package): 65585053108 ndc11 (package): 65585053104 ndc11 (package): 65585053103 ndc11 (package): 65585053101 spl id: 35bb7d72-6e4f-032f-e063-6394a90a0eba spl set id: 35bb7d59-111e-fa47-e063-6394a90aaf1e

Reported adverse events (FAERS/openFDA)#

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