SCAR ZONE BURN TOPICAL ANALGESIC AND ANTISEPTIC- lidocaine, benzalkonium chloride gel

Scar Zone Burn Topical Analgesic and Antiseptic by

Drug Labeling and Warnings

Scar Zone Burn Topical Analgesic and Antiseptic by is a Otc medication manufactured, distributed, or labeled by CCA Industries, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Lidocaine 2.00%
Benzalkonium Chloride 0.13%

Purpose

Topical Analgesic/Anesthetic
First Aid Antiseptic

Use

For temporary relief of pain or discomfort, for first degree burns or superficial second degree burns and to help prevent infection in: minor burns, cuts, scrapes.

Warnings

• For external use only

Do not use 

• for more than 1 week
• in or near eyes
• over an area larger than the palm of your hand

Ask a doctor before use if 

burn in severe

Ask a doctor or pharmacist before use if

• you have a history of heart disease or serious burns

Stop use and ask a doctor if 

increased redness or weeping or pain persist or clears up and occurs again within a few days

Keep out of reach of children

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

adults and children 2 years and over

• clean the affected area
• lightly apply to the affected area 1 to 3 times daily
• may be covered with a sterile bandage
• Children under 2 years, consult a doctor.

Inactive Ingredients

allantoin, allium cepa (onion) bulb extract, aloe barbadensis leaf juice, benzyl alcohol, butylene glycol, calophyllum tacamahaca (tamanu) seed oil, camellia sinensis leaf extract, centella asiatica extract, citric acid, glycerin, melaleuca alternifolia (tea tree) leaf oil, methylisothiazolinone, phenoxyethanol, phytonadione, polysorbate 60, propylene glycol, sodium polyacrylate, water (aqua).

Questions or Comments?

• Call 1-800-595-6230 

Package Labeling:

INGREDIENTS AND APPEARANCE

SCAR ZONE BURN TOPICAL ANALGESIC AND ANTISEPTIC 
lidocaine, benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 61543-6174
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
ONION (UNII: 492225Q21H)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BENZYL ALCOHOL (UNII: LKG8494WBH)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
TEA TREE OIL (UNII: VIF565UC2G)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PHYTONADIONE (UNII: A034SE7857)
POLYSORBATE 60 (UNII: CAL22UVI4M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 61543-6174-5	1 in 1 BOX	03/15/2019
1		14 g 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	06/14/2010

Labeler - CCA Industries, Inc. (106771041)