LIDOEASE 2%- lidocaine hcl 2% gel

Lidoease 2% by

Drug Labeling and Warnings

Lidoease 2% by is a Otc medication manufactured, distributed, or labeled by PureTek Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine HCl 2%

Purpose

Topical Analgesic

Uses

For the temporarily 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 ask a doctor if

■ If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use and consult a licensed healthcare practitioner.

Keep out of reach of children.

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

Directions:

■ Adults and children 2 years or older: Apply to affected area not more than 3 to 4 times daily.
■ Children under 2 years: do not use; consult a licensed healthcare practitioner.

Other information

■ Store at 20°-25°C (68°-77°F) [See USP controlled room temperature].Protect from freezing.

Inactive ingredients:

Aloe Barbadensis (Aloe Vera) Leaf Juice, Aqua (Purified Water), Caprylyl Glycol, Carbomer, Chlorphenesin, Cucumis Sativus (Cucumber) Fruit Extract, Dimethicone, Glycerin, Phenoxyethanol, Propanediol, Propylene Glycol, Sodium Hydroxide.

Lidoease™ 2% Gel

3 oz (85 g)


1 oz (28.35 g)

INGREDIENTS AND APPEARANCE

LIDOEASE 2% 
lidocaine hcl 2% gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59088-221
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	20 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CARBOMER (UNII: 0A5MM307FC)
CUCUMBER (UNII: YY7C30VXJT)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
CHLORPHENESIN (UNII: I670DAL4SZ)
GLYCERIN (UNII: PDC6A3C0OX)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59088-221-07	85 g in 1 TUBE; Type 0: Not a Combination Product	08/06/2025
2	NDC: 59088-221-03	28.35 g in 1 TUBE; Type 0: Not a Combination Product	04/16/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	08/06/2025

Labeler - PureTek Corporation (785961046)