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Lidocaine

Dosage form
CREAM
Labeler
Stratus Pharmaceuticals Inc
Label updated
2024-09-19
Retrieved
2026-09-07
Active ingredients
Lidocaine
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredient

Lidocaine 4% (4g in 100g)

Purpose

Local analgesic

Uses

for the temporary relief of pain and itching associated with

  • minor burns
  • sunburn
  • minor cuts
  • scrapes
  • insect bites
  • minor skin irritations
Warnings

For external use only

When using this product

  • avoid contact with the eyes
  • do not use in large quantities, particularly over raw surfaces or blistered areas

Stop use and consult a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days

Label information

Lidocaine is NOT approved by FDA to treat teething pain and should NOT be given to infants and young children for this use.

If pregnant or breast-feeding

Ask a health professional before use.

Label information

Keep out of reach of children. If accidentally ingested, get medical help or contact a Poison Control Center immediately.

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: do not use, consult a doctor.
Other information

Store at 20°C to 25°C (68°F to 77°F)

Inactive ingredients

acrylamide, allantoin, aloe vera extract, benzyl alcohol, c12-15 alkyl benzoate, carbomer, isohexadecane, polysorbate 80, propylene glycol, purified water, sodium acryloydimethyl taurate, sodium laureth sulfate, soy lecithin, tocopheryl acetate.

Questions?

Call us at (800) 442-7882

Label information

Distributed by:
Stratus Pharmaceuticals Inc.
Miami, FL 33186

PRINCIPAL DISPLAY PANEL - 28.35 g Tube Box

STRATUS
PHARMACEUTICALS INC

NDC 58980-824-30

Net WT. 1 oz. / 28.35 g

LIDOCAINE CREAM
4%

PAIN RELIEVING CREAM

FOR EXTERNAL USE ONLY.
NOT FOR OPHTHALMIC USE

[Image in the official label — see DailyMed source]

DailyMed Set ID: e1a8d4a7-01f7-4bab-8d09-875c461b3b61 · Version 2
NDC: 58980-824