WhiskCare 377

Manufacturer
Whisk Products, Inc.
Effective date
2024-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:19:33

Label at a glance#

ProductWhiskCare 377
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 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.
  • Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Propylene Glycol, Phenoxyethanol, Lauramine Oxide, Panthenol, Fragrance, 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
1038799benzalkonium chloride 0.1 % Topical FoamPSN1
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD1
1038799benzalkonium chloride 0.1 % Topical FoamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65585-529-01WhiskCare 37750 mL in 1 BOTTLE, PUMPSOLUTION501
65585-529-02WhiskCare 37750 mL in 1 BOTTLE, PUMPSOLUTION501
65585-529-02WhiskCare 37724 in 1 BOXSOLUTION241
65585-529-03WhiskCare 377208198 mL in 1 DRUMSOLUTION2081981
65585-529-04WhiskCare 3774 in 1 BOXSOLUTION41
65585-529-04WhiskCare 3771000 mL in 1 BAGSOLUTION10001
65585-529-05WhiskCare 3778 in 1 BOXSOLUTION81
65585-529-05WhiskCare 3771000 mL in 1 BAGSOLUTION10001
65585-529-06WhiskCare 377550 mL in 1 BOTTLE, PUMPSOLUTION5501
65585-529-06WhiskCare 3776 in 1 BOXSOLUTION61
65585-529-07WhiskCare 3773785 mL in 1 BOTTLE, PLASTICSOLUTION37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65585-529WHISKCARE 377 (BENZALKONIUM CHLORIDE) SOLUTION [WHISK PRODUCTS, INC.]1Current NDC, 11 package rows20240915_2204c224-e12a-81c6-e063-6294a90a9fa4.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65585-52965585-529-01, 65585-529-02, 65585-529-03, 65585-529-04, 65585-529-05, 65585-529-06, 65585-529-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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 377BENZALKONIUM CHLORIDEWhisk Products, Inc.2204c224-e12a-81c6-e063-6294a90a9fa42024-08-01WarningsExact identifier
ndc (package): 65585-529-04
ndc (package): 65585-529-03
ndc (package): 65585-529-01
ndc (package): 65585-529-02
ndc (package): 65585-529-07
ndc (package): 65585-529-06
ndc (package): 65585-529-05
ndc (product): 65585-529
ndc11 (package): 65585052906
ndc11 (package): 65585052907
ndc11 (package): 65585052902
ndc11 (package): 65585052905
ndc11 (package): 65585052903
ndc11 (package): 65585052904
ndc11 (package): 65585052901
spl id: 2204be42-078c-37e9-e063-6294a90a20ab
spl set id: 2204c224-e12a-81c6-e063-6294a90a9fa4

Reported adverse events (FAERS/openFDA)#

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