FDA.reportPublic FDA data

WhiskCare 377

Manufacturer
Whisk Products, Inc.
Effective date
2024-09-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:19:28

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Case Label - 4 x 1000 mL BagsCase Label - 4 x 1000 mL Bags

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038799benzalkonium chloride 0.1 % Topical FoamPSN3
1038799benzalkonium chloride 1 MG/ML Topical FoamSCD3
1038799benzalkonium chloride 0.1 % Topical FoamSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65585-356-01WhiskCare 37750 mL in 1 BOTTLE, PUMPSOLUTION503
65585-356-02WhiskCare 37724 in 1 BOTTLESOLUTION243
65585-356-02WhiskCare 37750 mL in 1 BOTTLE, PUMPSOLUTION503
65585-356-03WhiskCare 377208198 mL in 1 DRUMSOLUTION2081983
65585-356-04WhiskCare 3771000 mL in 1 BAGSOLUTION10003
65585-356-04WhiskCare 3774 in 1 BOXSOLUTION43
65585-356-05WhiskCare 3778 in 1 BOXSOLUTION83
65585-356-05WhiskCare 3771000 mL in 1 BAGSOLUTION10003
65585-356-06WhiskCare 377550 mL in 1 BOTTLE, PUMPSOLUTION5503
65585-356-06WhiskCare 3776 in 1 BOXSOLUTION63
65585-356-07WhiskCare 3776 in 1 BOXSOLUTION63
65585-356-07WhiskCare 3771750 mL in 1 BOTTLE, PUMPSOLUTION17503
65585-356-08WhiskCare 3773785 mL in 1 BOTTLE, PLASTICSOLUTION37853

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65585-356WHISKCARE 377 (BENZALKONIUM CHLORIDE) SOLUTION [WHISK PRODUCTS, INC.]3Current NDC, 13 package rows20240915_124b403f-d12e-6e5c-e063-6394a90a63f8.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65585-35665585-356-01, 65585-356-02, 65585-356-03, 65585-356-04, 65585-356-05, 65585-356-06, 65585-356-07, 65585-356-08

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
NameUNIIKind
ACETAMIDOETHOXYETHANOLLVX2APC4XRIACT
DIHYDROXYETHYL COCAMINE OXIDE8AR51R3BL5IACT
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATEH2KVQ74JM4IACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT

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.124b403f-d12e-6e5c-e063-6394a90a63f82024-09-13WarningsExact identifier
ndc (package): 65585-356-05
ndc (package): 65585-356-06
ndc (package): 65585-356-07
ndc (package): 65585-356-02
ndc (package): 65585-356-03
ndc (package): 65585-356-04
ndc (package): 65585-356-01
ndc (package): 65585-356-08
ndc (product): 65585-356
ndc11 (package): 65585035606
ndc11 (package): 65585035604
ndc11 (package): 65585035605
ndc11 (package): 65585035607
ndc11 (package): 65585035602
ndc11 (package): 65585035603
ndc11 (package): 65585035601
ndc11 (package): 65585035608
spl id: 2206420a-400e-3a5f-e063-6394a90a49fd
spl set id: 124b403f-d12e-6e5c-e063-6394a90a63f8

Reported adverse events (FAERS/openFDA)#

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