Fuzion AB Foam

Manufacturer
Zep Inc.
Effective date
2020-11-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:06:36

Label at a glance#

ProductFuzion AB Foam
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

For washing to decrease bacteria on hands.

Dosage and administration

Wet hands with water. Press pump to dispense product into hands. Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles. Rinse hands thoroughly and dry. Store at 20 to 25°C (68 to 77°F). Dispose in accordance with all applicable federal, state and local regulations.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial Hand Wash

Uses

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on hands.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.

When using this product

OTC - WHEN USING SECTION

  • Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands with water.
  • Press pump to dispense product into hands.
  • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
  • Rinse hands thoroughly and dry.
  • Store at 20 to 25°C (68 to 77°F).
  • Dispose in accordance with all applicable federal, state and local regulations.

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Lauryl/Myristyl Amidopropyl Amine Oxide, Glycerin, Di-PPG-2 Myreth-10 Adipate, Tetrasodium Iminodisuccinate, Methylchloroisothiazolinone, Methylisothiazolinone, Fragrance, Glutaral, Citric Acid, Red 4, Yellow 5

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-I-BUY-ZEP (1-800-428-9937)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-38866949-388-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

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
b463e5f6-1411-d413-e053-2a95a90ac33b5a910011-a7a4-d548-e053-2991aa0a93d92020-11-18WarningsExact identifier
spl id: b463e5f6-1411-d413-e053-2a95a90ac33b
spl set id: 5a910011-a7a4-d548-e053-2991aa0a93d9

Reported adverse events (FAERS/openFDA)#

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