WhiskCare 357

Manufacturer
Whisk Products, Inc.
Effective date
2025-05-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:01:07

Label at a glance#

ProductWhiskCare 357
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

Reduces amount of bacteria on hands 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 for at least fifteen seconds. Rinse with potable water.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Skin Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Reduces amount of bacteria on hands
  • 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 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

  • Pump a small amount of foam into palm of hand.
  • Rub thoroughly over all surfaces of both hands for at least fifteen seconds.
  • Rinse with potable water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Phenoxyethanol, Citric Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label - 1 Gallon Short Neck BottleProduct Label - 1 Gallon Short Neck Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapPSN2
1233282benzalkonium chloride 1 MG/ML Medicated Liquid SoapSCD2
1233282benzalkonium chloride 0.1 % Medicated Liquid SoapSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65585-558-01WhiskCare 35750 mL in 1 BOTTLE, PUMPSOLUTION502
65585-558-02WhiskCare 3571000 mL in 1 BAGSOLUTION10002
65585-558-02WhiskCare 3578 in 1 BOXSOLUTION82
65585-558-03WhiskCare 3576 in 1 BOXSOLUTION62
65585-558-03WhiskCare 3571750 mL in 1 BOTTLE, PUMPSOLUTION17502
65585-558-04WhiskCare 3573785 mL in 1 BOTTLE, PLASTICSOLUTION37852
65585-558-05WhiskCare 357208198 mL in 1 DRUMSOLUTION2081982
65585-558-06WhiskCare 3574 in 1 BOXSOLUTION42
65585-558-06WhiskCare 3571000 mL in 1 BAGSOLUTION10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65585-558WHISKCARE 357 (BENZALKONIUM CHLORIDE) SOLUTION [WHISK PRODUCTS, INC.]2Current NDC, 9 package rows20250519_2f23296e-8520-b2e2-e063-6294a90a3e9e.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65585-55865585-558-01, 65585-558-02, 65585-558-03, 65585-558-04, 65585-558-05, 65585-558-06

Ingredients#

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

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

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
WhiskCare 357BENZALKONIUM CHLORIDEWhisk Products, Inc.2f23296e-8520-b2e2-e063-6294a90a3e9e2025-05-14WarningsExact identifier
ndc (package): 65585-558-02
ndc (package): 65585-558-03
ndc (package): 65585-558-05
ndc (package): 65585-558-04
ndc (package): 65585-558-01
ndc (package): 65585-558-06
ndc (product): 65585-558
ndc11 (package): 65585055803
ndc11 (package): 65585055806
ndc11 (package): 65585055801
ndc11 (package): 65585055805
ndc11 (package): 65585055804
ndc11 (package): 65585055802
spl id: 35447191-995d-2ef0-e063-6394a90aff7a
spl set id: 2f23296e-8520-b2e2-e063-6294a90a3e9e

Reported adverse events (FAERS/openFDA)#

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