ANTIBIOTIC FREE WOUND GEL AND PAIN RELIEF- benzalkonium chloride and lidocaine hydrochloride gel

Antibiotic Free Wound Gel and Pain Relief by

Drug Labeling and Warnings

Antibiotic Free Wound Gel and Pain Relief by is a Otc medication manufactured, distributed, or labeled by ASO LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Lidocaine Hydrochloride 2.00%

Purpose

first aid antiseptic

external analgesic

Uses

• First aid to help prevent infection in minor cuts, scrapes and burns
• For the temporary relief of pain associated with minor burns

Warnings

For external use only

Do not use

• in the eyes
• over large areas of the body, particularly over raw surfaces or blistered areas
• longer than a week unless directed by a doctor

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

Stop use and ask a doctor if

• the condition persists more than 7 days or gets worse
• condition clears up and occurs again within a few days

Keep out of reach of children.

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Directions

• Clean the affected area
• adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
• children under 2 years of age: consult a doctor
• may be covered with a sterile bandage
• if bandaged, let dry first

Other information

• Store at room temperature

Inactive ingredients

caprylyl glycol, chlorphenesin, edetate disodium, glycerin, hydroxyethyl cellulose, phenoxyethanol, polysorbate 20, purified water

Principal Display Panel

Antibacterial

Lidocaine Wound Gel

LIDOCAINE HYDROCHLORIDE, 2%
BENZALKONIUM CHLORIDE, 0.13%

Antibacterial Gel with Pain Relief Helps Prevent Infection

• Antibiotic Free
• For treating minor cuts, scrapes & burns
• Water-based clear hydrogel
• Helps reduce scarring

NET WT 0.5 OZ (14 g)

INGREDIENTS AND APPEARANCE

ANTIBIOTIC FREE WOUND GEL AND PAIN RELIEF 
benzalkonium chloride and lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51142-352
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2 g  in 100 mL
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
CHLORPHENESIN (UNII: I670DAL4SZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51142-352-32	1 in 1 CARTON	03/21/2017
1		28 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 51142-352-14	1 in 1 CARTON	10/18/2019
2		14 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/21/2017

Labeler - ASO LLC (152793493)