Iron Company Heavy-Duty Sanitizing Alcohol Free Wipes Fresh Lemon Scent

Iron Company Heavy Duty Sanitizing Alcohol Free Wipes Fresh Lemon Scent by

Drug Labeling and Warnings

Iron Company Heavy Duty Sanitizing Alcohol Free Wipes Fresh Lemon Scent by is a Otc medication manufactured, distributed, or labeled by Ironcompany.com, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

IRON COMPANY HEAVY DUTY SANITIZING ALCOHOL FREE WIPES FRESH LEMON SCENT- benzalkonium chloride cloth 
Ironcompany.com, LLC

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Iron Company Heavy-Duty Sanitizing Alcohol Free Wipes Fresh Lemon Scent

DRUG FACTS

ACTIVE INGREDIENTS

Benzalkonium chloride 0.13%

Purpose

Antiseptic

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.

WARNINGS

For external use only
May irritate eyes

Keep out of the reach of children

unless under adult supervision

DIRECTIONS

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

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 Labeling:81197-000-05

IRON COMPANY HEAVY DUTY SANITIZING ALCOHOL FREE WIPES FRESH LEMON SCENT 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81197-000
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81197-000-08	800 in 1 BAG	12/15/2020	02/01/2023
1		4.1 mL in 1 PATCH; Type 0: Not a Combination Product
2	NDC: 81197-000-05	800 in 1 CANISTER	12/15/2020	02/01/2023
2		4.1 mL in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	12/15/2020	02/01/2023

Labeler - Ironcompany.com, LLC (004628657)

Revised: 12/2023

Document Id: 0bb9d365-f45f-deb2-e063-6294a90a9b21

34390-5

Set id: b60cb560-b85d-b8b7-e053-2995a90a7d6b

Version: 3

Effective Time: 20231204