LIDOCAINE 4% PATCH- lidocaine 4% patch 
SOLA Pharmaceuticals

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Lidocaine 4% Patch

Active Ingredients

Lidocaine

Purpose

Topical Anesthetic

Uses

For the temporary relief of pain

Warnings

For external use only

Do not use

When using this product

Stop use and ask a doctor if

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 12 years of age and over:

Children under 12 years of age: consult a doctor

Other Information

Other Ingredients

Dihydroxyaluminum Aminoacetate, Disodium Ethylenediaminetetraacetic Acid, Glycerin, Kaolin, Methylparaben, Polysorbate 80, Propylene Glycol, Polyacrylic Acid, Polyvinylpyrrolidone K90, Propylparaben, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Water.

Questions or comments? 866-747-7365

Lidocaine 4% Patch

NDC 70512-812-30

Qty: 30 patches

Manufactured for:

SOLA Pharmaceuticals

Baton Rouge, LA 70810

Made in China

box

LIDOCAINE 4% PATCH 
lidocaine 4% patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70512-812
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
GLYCERIN (UNII: PDC6A3C0OX)  
DISODIUM ETHYLENEDIAMINEDIACETATE (UNII: EQL53S5L0F)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
KAOLIN (UNII: 24H4NWX5CO)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
POVIDONE K90 (UNII: RDH86HJV5Z)  
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
TARTARIC ACID (UNII: W4888I119H)  
Product Characteristics
Color    Score    
ShapeRECTANGLESize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70512-812-3030 in 1 BOX10/12/2023
11 g in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)10/12/2023
Labeler - SOLA Pharmaceuticals (080121345)

Revised: 5/2024
Document Id: 18e5c949-ca7c-2b48-e063-6294a90a2164
Set id: 078bc9a3-41b7-26a4-e063-6394a90a200d
Version: 4
Effective Time: 20240520
 
SOLA Pharmaceuticals