NEUROCAINE- lidocaine patch

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredients

Lidocaine 4%

Purposes

Topical analgesic

Uses

For the temporary relief of pain

Warnings

For external use only

Do Not Use

• If you are allergic to Lidocaine   
• On open wounds or on damaged, broken or irritated skin
• Remove immediately if you sense a burning sensation after application

When using this product:

• Do not use other topical products.
• Do not allow contact with eyes or mucous membranes
• Keep away from excessive heat.
• Do not apply heating pad to area of use.
• Apply only to clean, dry, untreated skin.
• Use only as directed. Read and follow all directions and warnings on this label.

Stop use and ask a doctor if:

• Condition worsens
• Symptoms persist for more than 7 days

If pregnant or breast-feeding,

Ask a physician before use.

Keep out of reach of children

If put in mouth, get medical help or contact a poison control center right away. Dispose of used product away from children and pets.

Directions

Adult and children 12 years of age and over:

• Clean and dry affected area
• Peel patch off plastic liner and place patch on affected area for no more than 12 hours
• Wash hands after applying patch
• Under age 12, consult a physician before use
• For easier removal of the patch, apply rubbing alcohol or baby oil to adhesive edge while gently peeling

Children under 12 years of age: Consult a doctor

Storage

• Store at 68-77℉ (20-25℃) - Room Temperature
• Do not exceed 100 oF (38 oC)

Inactive Ingredients

Acrylic Adhesive, Polyethylene Fabric

Questions?

Call: 813-380-0271

Label

INGREDIENTS AND APPEARANCE

NEUROCAINE 
lidocaine patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85622-501
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	40 mg  in 40 mg

Inactive Ingredients
Ingredient Name	Strength
ACRYLIC ACID (UNII: J94PBK7X8S)

Product Characteristics
Color		Score
Shape	RECTANGLE (Patch)	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85622-501-15	15 in 1 BOX	04/16/2026
1		1 mg in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/16/2026

Labeler - Blue Heron Pharmaceuticals LLC (137019051)