BACTINE MAX- bactine max wound wash liquid 
WellSpring Pharmaceutical Corporation

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BACTINE MAX WOUND WASH

Active ingredient

Benzalkonium Cl 0.13% w/w

Purpose

First aid antiseptic

Use

First aid to help prevent bacterial contamination or skin infection in minor cuts, scrapes and burns.

Warning

For external use only. Do not use on or near the eyes. Do not apply to large areas of the body. Ask a doctor before use if -you have - deep or puncture wounds - animal bites - serious burns. Stop use and ask doctor if - condition persists or get worse - symptoms persist for more than 7 days.

For external use only

For external use only

Do not use

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

When using this product

Stop use and ask a doctor if

Pregnancy/breast-feeding warning

Keep out of reach of children

Directions

Clean the affected area, apply a small amount of this product on the area 1 to 3 times daily; may be covered with a sterile bandage (let dry first).

Other information

Avoid excessive heat

Inactive ingredients

aloe barbadensis leaf extract, edetate disodium, PEG-100 Stearate, propylene glycol, purified water

Questions?

1-844-241-5454 Mon-Fri (8-5 EST) or bactine.com

Bactine Wound Wash Label

Bactine Max Wound Wash IFC Label - CT82080B

Bactine Max Wound Wash IFC Label


BACTINE  MAX
bactine max wound wash liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65197-820
Route of AdministrationCUTANEOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65197-820-801 in 1 CARTON04/15/2023
1236 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00304/15/2023
Labeler - WellSpring Pharmaceutical Corporation (110999054)

Revised: 10/2020
Document Id: f70cb59a-aa61-415b-8449-c3318787c92d
Set id: 39b26c28-93e0-41a9-8018-f73525ebc015
Version: 6
Effective Time: 20201029
 
WellSpring Pharmaceutical Corporation