Iron Company Heavy Duty Sanitizing Alcohol Free Wipes Fresh Lemon Scent

Manufacturer
Ironcompany.com, LLC
Effective date
2021-01-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:54:25

Label at a glance#

ProductIron Company Heavy Duty Sanitizing Alcohol Free Wipes Fresh Lemon Scent
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

• For hand sanitizing to decrease bacteria on the skin. • Apply topically to the skin to help prevent cross contamination. • Recommended for repeated use. • Dries in seconds.

Dosage and administration

• Tear V notch on top of plastic bag. • Pull first wipe from the center of roll up through opening of bag. • Thread first wipe through the dispensing nozzle in lid of floor stand or dispenser. • Close dipenser door. Wipe dispensing tension may be adjusted on top of dispenser. Dispenser must be mounted with wipes dispensing up.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

• For hand sanitizing to decrease bacteria on the skin.
• Apply topically to the skin to help prevent cross contamination.
• Recommended for repeated use.
• Dries in seconds.

WARNINGS

WARNINGS SECTION

• For external use only
• May irritate eyes

Keep out of the reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

unless under adult supervision

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

• Tear V notch on top of plastic bag.
• Pull first wipe from the center of roll up through opening of bag.
• Thread first wipe through the dispensing nozzle in lid of floor stand or dispenser.
• Close dipenser door. Wipe dispensing tension may be adjusted on top of dispenser. Dispenser must be mounted with wipes dispensing up.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua), Propylene Glycol, Polysorbate 20, Disodium Cocoamphodiacetate, Citric Acid, Disodium EDTA, Potassium Sorbate,
Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E), Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

Package Labeling:81197-000-05

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81197-00081197-000-08, 81197-000-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
0bb9d365-f45f-deb2-e063-6294a90a9b21b60cb560-b85d-b8b7-e053-2995a90a7d6b2023-12-04WarningsExact identifier
spl set id: b60cb560-b85d-b8b7-e053-2995a90a7d6b

Reported adverse events (FAERS/openFDA)#

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