LIDOCAINE HYDROCHLORIDE 2%- lidocaine hydrochloride gel

Lidocaine Hydrochloride 2% by

Drug Labeling and Warnings

Lidocaine Hydrochloride 2% by is a Otc medication manufactured, distributed, or labeled by Aldermed Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lidocaine Hydrochloride 2%

Purpose

External Analgesic

Use(s)

■ For the temporary relief of pain associated with ■ Minor burns ■ Sunburn

Warnings

For External Use Only

Do not use

■ On wounds or damaged skin

■ In large quantities, particularly over raw surfaces or blistered areas

When using this product

■ Avoid contact with the eyes

■ Do not bandage tightly

Stop use and ask a doctor if

■ Condition worsens

■ Symptoms persist for more than 7 days

■ Symptoms clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)

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

Other Information

Store at room temperature

Tamper Evident. Do not use if seal is torn, cut, or opened.

• See sachet or cartonfor lot number and expiry date

Inactive Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosscopolymer, Carbomer, Glycerin, Imidurea, Methylparaben, Propylene Glycol, Propylparaben, Purified Water, Tea Tree Leaf Oil, Trolamine

Questions?

1-888-396-2739 Monday - Friday, 9AM - 5PM EST

Label

INGREDIENTS AND APPEARANCE

LIDOCAINE HYDROCHLORIDE 2% 
lidocaine hydrochloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87236-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
TROLAMINE (UNII: 9O3K93S3TK)
METHYLPARABEN (UNII: A2I8C7HI9T)
GLYCERIN (UNII: PDC6A3C0OX)
IMIDUREA (UNII: M629807ATL)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
TEA TREE OIL (UNII: VIF565UC2G)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
CARBOMER 940 (UNII: 4Q93RCW27E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87236-015-35	25 in 1 BOX	01/01/2026
1		3.5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/01/2026

Labeler - Aldermed Inc. (144887712)