BURN CREAM- tetracaine cream 
Bio-Medical & Pharmaceutical Manufacturing Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Topical Burn Cream Plus Pain Relief

Active Ingredient

Active Ingredient Purpose

Tetracaine (1.0%).......................Pain & Itch Relief

Purpose

• For temporary relief of minor aches and pains of muscles and joints commonly assoicated with backache, arthritis, strains, bruises, sprains, and burns.

Indications

• For cooling, deep-penetrating pain relief, apply a thin layer sparingly to affected areas.
• Apply up to 3 times daily.

Warnings

• Not for use on children under 2 years old except as directed by
a doctor.
• Avoid contact with the eyes.
• For external use only.
• If irritation develops and persists, discontinue use and consult a
doctor.
• If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use and consult a doctor.












KEEP OUT OF REACH OF CHILDREN

Directions

• Apply this product topically to affected areas.
• Use up to 3 times daily.
• Use only as directed.

Other Information

External Anesthetic

Inactive Ingredients

Water, Stearic Acid, Lauramide DEA, Beeswax, Propylene Glycol, Sodium Tetraborate, Sodium Lauryl Sulfate, Diazolidinyl Urea, Methylparaben, Propylparaben, Triethanolamine, Eucalyptus Oil.

Questions or Comments

Bio-Medical & Pharm. Mfg. Corp.
4311 South Dr., Houston, TX 77053-4820
281.835.8051 www.bio-medicalmanufacturing.com

Burn cream

BURN CREAM 
tetracaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37945-212
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TETRACAINE (UNII: 0619F35CGV) (TETRACAINE - UNII:0619F35CGV) TETRACAINE10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
YELLOW WAX (UNII: 2ZA36H0S2V)  
SODIUM BORATE ANHYDROUS (UNII: 8191EN8ZMD)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
TROLAMINE (UNII: 9O3K93S3TK)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:37945-212-3512 in 1 BOX08/19/2016
1NDC:37945-212-3410 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34808/19/2016
Labeler - Bio-Medical & Pharmaceutical Manufacturing Corporation (072186356)
Establishment
NameAddressID/FEIBusiness Operations
Bio-Medical & Pharmaceutical Manufacturing Corporation072186356manufacture(37945-212)

Revised: 12/2019
Document Id: 9a00dfce-2ac0-1632-e053-2995a90a3f4a
Set id: 3a477714-6ff3-62aa-e054-00144ff8d46c
Version: 2
Effective Time: 20191218
 
Bio-Medical & Pharmaceutical Manufacturing Corporation