WhiskCare 377

Manufacturer: Whisk Products, Inc.
Effective date: 2024-08-28
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 00:17:53

Label at a glance#

ProductWhiskCare 377 Free

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

Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

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 avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor ifirritation 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

Pump a small amount of foam into palm of hand.
Rub thoroughly over all surfaces of both hands.
Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl PG-Dimonium Chloride Phosphate, Dihydroxyethyl Cocamine Oxide, Acetamidoethoxyethanol, Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 Gallon Product Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1038799	benzalkonium chloride 0.1 % Topical Foam	PSN	4
1038799	benzalkonium chloride 1 MG/ML Topical Foam	SCD	4
1038799	benzalkonium chloride 0.1 % Topical Foam	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
65585-527-01	WhiskCare 377Free	8 in 1 BOX	SOLUTION	8	4
65585-527-01	WhiskCare 377Free	1000 mL in 1 BAG	SOLUTION	1000	4
65585-527-02	WhiskCare 377Free	3785 mL in 1 BOTTLE, PLASTIC	SOLUTION	3785	4
65585-527-03	WhiskCare 377Free	1000 mL in 1 BAG	SOLUTION	1000	4
65585-527-03	WhiskCare 377Free	4 in 1 BOX	SOLUTION	4	4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
65585-527	WHISKCARE 377 FREE (BENZALKONIUM CHLORIDE) SOLUTION [WHISK PRODUCTS, INC.]	4	Current NDC, 5 package rows	20240829_0bf163a6-0239-932c-e063-6394a90a12ab.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

WhiskCare 377 Free
Benzalkonium Chloride
WATER
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE
DIHYDROXYETHYL COCAMINE OXIDE
ACETAMIDOETHOXYETHANOL
CITRIC ACID MONOHYDRATE
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65585-527	65585-527-01, 65585-527-02, 65585-527-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE	H2KVQ74JM4	IACT
DIHYDROXYETHYL COCAMINE OXIDE	8AR51R3BL5	IACT
ACETAMIDOETHOXYETHANOL	LVX2APC4XR	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	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
WhiskCare 377 Free	BENZALKONIUM CHLORIDE	Whisk Products, Inc.	0bf163a6-0239-932c-e063-6394a90a12ab	2024-08-28	Warnings	Exact identifier ndc (package): 65585-527-01 ndc (package): 65585-527-03 ndc (package): 65585-527-02 ndc (product): 65585-527 ndc11 (package): 65585052701 ndc11 (package): 65585052702 ndc11 (package): 65585052703 spl id: 20c2ed0e-0c2b-b0bb-e063-6394a90a73e6 spl set id: 0bf163a6-0239-932c-e063-6394a90a12ab

Reported adverse events (FAERS/openFDA)#

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