PROCURE ANTISEPTIC WOUND CLEANSER- benzethonium chloride 0.13% spray

ProCure Antiseptic Wound Cleanser by

Drug Labeling and Warnings

ProCure Antiseptic Wound Cleanser by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzathonium Chloride 0.13%

Purpose

First Aid Antiseptic

Uses

Uses

First aid to help prevent skin infection in minor cuts, scrapes or burns

Warnings

Warnings

For External Use Only

Do Not Use

Do not use

• In the eyes or over large areas of the body
• Longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

Stop use and ask a doctor

Stop use and ask a doctor if condition persists or gets worse

Keep out of reach of children

Keep out of reach of children. In case of accidental ingestion, contact a physician or Poison Control Center right away.

Directions

Directions

• Cleanse affected area
• Spray a small mount of this product on the area 1 to 3 times daily
• May be covered with a sterile bandage
• If bandaged, let dry first

Inactive Ingredients

Inactive Ingredients: Benzyl Alcohol, Edetate Disodium, Glycerin, Polyquaternium-10, Polysorbate 20, Purified Water, Sodium Citrate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE ANTISEPTIC WOUND CLEANSER 
benzethonium chloride 0.13% spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL (UNII: LKG8494WBH)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
POLYQUATERNIUM-10 (125 MPA.S AT 2%) (UNII: L45WU8S981)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-052-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/08/2026

Labeler - Twin Med LLC (009579330)