BACTINE MAX- bactine max wound wash liquid

BACTINE by

Drug Labeling and Warnings

BACTINE by is a Otc medication manufactured, distributed, or labeled by WellSpring Pharmaceutical Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

INGREDIENTS AND APPEARANCE

BACTINE  MAX
bactine max wound wash liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65197-820
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
PEG-100 STEARATE (UNII: YD01N1999R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65197-820-80	1 in 1 CARTON	04/15/2023
1		236 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/15/2023

Labeler - WellSpring Pharmaceutical Corporation (110999054)