Summit E2 Foaming E2

Manufacturer
Dyno Manufacturing
Effective date
2022-11-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:48:09

Label at a glance#

ProductSummit E2 Foaming E2
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Indications and uses

For hand washing to help reduce bacteria on the skin

Dosage and administration

Pump onto dry hands Lather vigorously for at least 15 seconds. Rinse and dry thoroughly

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

For external use only.

Do Not Use

OTC - DO NOT USE SECTION

In children less that 2 months of age
on open skin wounds

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be signs of a serious condition.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

Pump onto dry hands
Lather vigorously for at least 15 seconds.
Rinse and dry thoroughly

Other Information

OTHER SAFETY INFORMATION

Store between 15-30C (59-86F)
Avoid Freezing and excessive heat above 40C (104F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cetrimonium chloride, Lauramine Oxide, Glycerin, Citric Acid, Cocamidopropyl PG-Dimonium Chloride Phosphate, Tetrasodium EDTA

Summit E2 Foaming E2 Hand Soap

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79532-02179532-021-85

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
ed364ad8-d5eb-4366-e053-2995a90a2714ed365898-e1b2-3f2d-e053-2995a90a11d42022-11-11WarningsExact identifier
spl id: ed364ad8-d5eb-4366-e053-2995a90a2714
spl set id: ed365898-e1b2-3f2d-e053-2995a90a11d4

Reported adverse events (FAERS/openFDA)#

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