Alpha Foaming E-2

Manufacturer: Whisk Products, Inc.
Effective date: 2025-06-23
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: legacy-cache
Hydrated at: 2026-08-01 20:36:41

Label at a glance#

ProductAlpha Foaming E-2

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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 · 7 matching rows.

Alpha Foaming E-2
Benzalkonium Chloride
PEG-120 METHYL GLUCOSE DIOLEATE
WATER
LAURAMINE OXIDE
GLYCERIN
BENZALKONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
65585-514	65585-514-01, 65585-514-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PEG-120 METHYL GLUCOSE DIOLEATE	YM0K64F20V	IACT
WATER	059QF0KO0R	IACT
LAURAMINE OXIDE	4F6FC4MI8W	IACT
GLYCERIN	PDC6A3C0OX	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
38447cb6-b56f-b7f4-e063-6294a90a1acc			637cb6b7-2fbf-49fe-910c-aaf4b7e64edc	2025-06-23	Warnings	Exact identifier spl id: 38447cb6-b56f-b7f4-e063-6294a90a1acc spl set id: 637cb6b7-2fbf-49fe-910c-aaf4b7e64edc

Reported adverse events (FAERS/openFDA)#

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