WOUND CLEANSER- wound cleanser spray 
Dynarex Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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3005 DynaWound Wound Cleanser Spray NDC 67777-403-01

Active Ingredient

Benzethonium Chloride 0.13%

Purpose

First Aid Antibiotic

Use(s)

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

Warnings

For External Use Only

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

deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

if condition persists or gets worse.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

• Clean the affected area

• Spray a small amount of this product on the area 1 to 3 times daily

• May be covered with a sterile bandage

• If bandaged let dry first

Other Information

• Store at room temperature 15°-30ºC (59º-86ºF)

• Avoid excessive heat

Inactive ingredients

Benzyl Alcohol, Disodium Edetate, Glycerin, Polyquaternium 10, Polysorbate 20, Purified Water, Sodium Citrate.

Label

3005-IN-MASTER

WOUND CLEANSER 
wound cleanser spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-403
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BENZYL ALCOHOL (UNII: LKG8494WBH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYQUATERNIUM-10 (125 MPA.S AT 2%) (UNII: L45WU8S981)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-403-0224 in 1 CASE02/13/2017
1NDC:67777-403-01236.5 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/13/2017
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 2/2023
Document Id: f3ccba46-0781-4b2e-e053-2a95a90ac043
Set id: 6a4dd82a-6b06-426b-9afd-415a1a4339b4
Version: 4
Effective Time: 20230203
 
Dynarex Corporation