ZEE BURN RELIEF- burn relief spray

Zee Burn Relief by

Drug Labeling and Warnings

Zee Burn Relief by is a Otc medication manufactured, distributed, or labeled by Cintas Corp, WaterJel Technologies. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Benzalkonium chloride 0.13%

Lidocaine hydrochloride 2.0%

Purposes

First aid antiseptic

Anesthetic

Uses

first aid to help prevent infection and relieve pain in minor burns

Warnings

For external use only.

Do not use

• in the eyes
• over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use if you have a serious burn

Stop use and ask a doctor if the condition lasts or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• shake well before using
• clean the affected area
• spray a small amount on the area 1 to 3 times daily
• may be covered with a sterile bandage. If bandaged, let dry first.

Inactive ingredients

diazolidinyl urea, edetate disodium, glycerin, hydroxypropyl methylcellulose, methylparaben, octoxynol 9, propylparaben, purified water, tea tree oil, trolamine

Questions?

1-800-327-2704 or zeemedical.com

Principal Display Panel

BURN RELIEF SPRAY

First Aid

Antiseptic/Anesthetic

Treats minor burns

Relieves pain

Helps prevent infection

2 fl oz (59 ml)

ZEE®

Distributed by Zee Medical Distributors, LLC

Mason, OH 45040

1805

INGREDIENTS AND APPEARANCE

ZEE BURN RELIEF 
burn relief spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 100 mL
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
METHYLPARABEN (UNII: A2I8C7HI9T)
OCTOXYNOL-9 (UNII: 7JPC6Y25QS)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
TEA TREE OIL (UNII: VIF565UC2G)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-030-01	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/26/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	04/26/2022

Labeler - Cintas Corp (056481716)

Establishment
Name	Address	ID/FEI	Business Operations
WaterJel Technologies		155522589	manufacture(42961-030)