curacaine description, usages, side effects, indications, overdosage, supplying and lots more!

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curacaine

Transdermal Corp
Transdermal Corp




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients

Lidocaine 4%

Purpose

PURPOSE:

topical analgesic

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

Uses

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 Sulfate, Steric Acid, Tetrasodium EDTA, Tocopheryl Acetate, Sodium Hydroxide.

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

curacaine

curacaine

curacaine

Lidocaine CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:51350-010
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LIDOCAINE LIDOCAINE 40 mg

Inactive Ingredients

Ingredient Name Strength
CAPRYLYL GLYCOL
CETOSTEARYL ALCOHOL
CYCLOMETHICONE 5
GLYCERIN
Hexylene Glycol
PHENOXYETHANOL
POLYSORBATE 20
POLYSORBATE 60
propylene glycol
Jojoba Oil
HYALURONATE SODIUM
SODIUM LAURYL SULFATE
EDETATE SODIUM
.ALPHA.-TOCOPHEROL ACETATE
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:51350-010-01 30 in 1 TUBE
2 NDC:51350-010-51 1 in 1 BOX

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-09-12


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Be sure to consult your doctor before taking any medication!
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