Lidocaine HCl 3% Topical Anesthetic Cream

Manufacturer
Brookfield Pharmaceuticals, LLC
Effective date
2021-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:27:12

Label at a glance#

ProductLidocaine HCl
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure11 sections

Indications and uses

Temporarily relieves pain and itching due to minor cuts sunburn minor scrapes minor burns insect bites minor skin irritations

Dosage and administration

Adults and children 2 years and older apply externally to the affected area up to 3 to 4 times a day Children under 2 years ask a doctor

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 3% w/w

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves pain and itching due to

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

Warnings

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

  • Do not use in or near the eyes
  • Do not use in large quantities, particularily over raw surfaces or blistered areas

Stop use and ask a doctor if

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • allergic reaction occurs
  • condition worsens or does not improve in 7 days
  • symptoms clear up and return within a few days
  • redness, irritation, swelling, pain or other symptoms begin or increase

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years and olderapply externally to the affected area up to 3 to 4 times a day

Children under 2 years ask a doctor

Other information

OTHER SAFETY INFORMATION

  • May be applied under occlusive dressing.
  • Store at 20-25°C (68-77°F); excursions permitted to 15-30°C (59-86°F). See USP Controlled Room Temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzyl alcohol, carbomer, cholesterol, lecithin, polysorbate 80, propylene glycol, purified water, sodium hydroxide, titanium dioxide, tocopheryl acetate.

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage LabelPackage LabelPackage Label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71351-018-01GM - Gram71351-018e2a0837c-54cf-42be-a0c4-5d4562e949ab12019-12-10
71351-018-03GM - Gram71351-01831a085bf-149e-4bba-bbb6-aede898e575112019-12-10

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71351-01871351-018-01, 71351-018-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
d0eb2ff4-e906-2be5-e053-2a95a90af3d697b5a1f3-6d94-216c-e053-2a95a90aa1892021-11-16WarningsExact identifier
spl id: d0eb2ff4-e906-2be5-e053-2a95a90af3d6
spl set id: 97b5a1f3-6d94-216c-e053-2a95a90aa189

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.