LIDOCAINE PAIN RELIEF GEL PATCH- lidocaine pain relief patch 
Dynarex

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1454 Lidocaine Pain Relief Gel-Patch NDC 67777-009-40

Active Ingredients

Lidocaine 4%

Puropose

Topical anesthetic

Use

For temporary relief of pain

Warnings

For external use only

Do not use

  • more than 1 patch at a time
  • on wounds or damaged skin
  • with a heating pad
  • if you are allergic to any ingredients of this product

When using this product

  • use only as directed
  • avoid contact with the eyes, mucous membranes or rashes
  • do not bandage tightly

Stop use and ask a doctor if

  • localized skin reactions, such as rash, itching, redness, pain, swelling and blistering develop
  • conditions worsen
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

if pregnant or breast feeding

ask a health 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

Inactive Ingredients

Dihydroxyaluminum Aminoacetate, Glycerol, Kaolin, Methylparaben, Polyacrylic Acid (250000 MW), Polysorbate 80, Povidone K90, Propylene Glycol, Propylparaben, Sodium Polyacrylate (2500000 MW), Tartaric Acid, Titanium Dioxide, Water

Questions?

1-888-DYNAREX

1454 BX Master

LIDOCAINE PAIN RELIEF GEL PATCH 
lidocaine pain relief patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
GLYCERIN (UNII: PDC6A3C0OX)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
POVIDONE K90 (UNII: RDH86HJV5Z)  
KAOLIN (UNII: 24H4NWX5CO)  
TARTARIC ACID (UNII: W4888I119H)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-009-4060 in 1 CASE08/27/2019
1NDC:67777-009-395 in 1 BOX
140 mg in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01708/27/2019
Labeler - Dynarex (008124539)
Registrant - Dynarex (008124539)

Revised: 3/2024
Document Id: 13b2ca0b-949a-bcd0-e063-6394a90a5b26
Set id: 960e4240-cd09-2560-e053-2a95a90a7bcf
Version: 9
Effective Time: 20240315
 
Dynarex