FDA.reportPublic FDA data

Ultra Professional Antibacterial Foaming Hand

Manufacturer
Whisk Products, Inc.
Effective date
2019-04-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:25:37

Label at a glance#

ProductUltra Professional Antibacterial Foaming Hand
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Apply a palmful to hands and forearms. Scrub thoroughly for at least 15 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 15 seconds.
  • Rinse completely and dry.

​Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance, Yellow 5, Blue 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Case Label (8 x 1000 mL Bags)Case Label (8 x 1000 mL Bags)

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
65585-58465585-584-01

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
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
WATER059QF0KO0RIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
GLYCERINPDC6A3C0OXIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT

Source Document#

Source XML · Source PDF

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
f7fb0f16-5338-ff03-e053-6294a90aebaea175f9ce-ccdf-4c21-a4f4-ac79afee38ee2023-03-28WarningsExact identifier
spl set id: a175f9ce-ccdf-4c21-a4f4-ac79afee38ee

Reported adverse events (FAERS/openFDA)#

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