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CURACAINE

Dosage form: cream
Ingredients: LIDOCAINE 4g in 100mL
Labeler: Transdermal Corp
NDC code: 51350-011

Medically reviewed by Drugs.com. Last updated on Apr 5, 2024.

Active Ingredients

Lidocaine 4%

PURPOSE:

topical analgesic

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

Uses for the temporary relief of

  • pain and itching
  • insect bites
  • sunburn
  • minor cuts
  • scrapes
  • burns
  • minor skin irritations

Warnings

For external use only

When using this product

  • Keep out of eyes. Rinse with water to remove.
  • Do not use in large quantities, particularly over raw surfaces or blistered areas.
  • If pregnant or breast feeding, ask a health professional before use.

Directions

Adults and children 2 years of age and older:

Apply to affected area not more than 3 to 4 times daily.

Children under 2 years of age: consult a doctor.

Inactive Ingredients

Caprylyl Glycol, Cetearyl Alcohol, Clyclopentasiloxane, Deionized water, Dimethyl Sulone, Glycerin, Hexylene Glycol, Phenoxyethanol, Polysorbate 20, Polysorbate 60, Propylene Glycol, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium hyaluronate, Sodium Lauryl Sulfate, Stearic Acid, Tetrasodium EDTA, Tocopheryl Acetate

Stop use and ask a doctor if conditions worsens, or, if symptoms persist for more than 7 days, or clear up and occur again within a few days, discontinue use of the product and consult a doctor.

CURACAINE 
lidocaine cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51350-011
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (LIDOCAINE) LIDOCAINE4 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAPRYLYL GLYCOL 
CETOSTEARYL ALCOHOL 
CYCLOMETHICONE 5 
WATER 
DIMETHYL SULFONE 
GLYCERIN 
HEXYLENE GLYCOL 
PHENOXYETHANOL 
POLYSORBATE 20 
POLYSORBATE 60 
PROPYLENE GLYCOL 
JOJOBA OIL 
HYALURONATE SODIUM 
SODIUM LAURYL SULFATE 
STEARIC ACID 
EDETATE SODIUM 
.ALPHA.-TOCOPHEROL ACETATE 
Packaging
#Item CodePackage Description
1NDC:51350-011-511 TUBE in 1 BOX
1NDC:51350-011-0130 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/03/2015
Labeler - Transdermal Corp (963383612)
Registrant - Transdermal Corp (963383612)

Revised: 04/2015
 
Transdermal Corp

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.