LIDOCAINE TATTOO WIPE- lidocaine hydrochloride cloth

Lidocaine Tattoo Wipe by

Drug Labeling and Warnings

Lidocaine Tattoo Wipe by is a Otc medication manufactured, distributed, or labeled by MD Tattoo Company, Diamond Wipes International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

LIDOCAINE HCI 3% w/w

Purpose

Pain reliever

Uses

For temporarily relief of pain and itching associated with minor cuts burns sunburns insect bites scrapes and minor skin irritations

Warnings

For external use only.

Ask a doctor if you have deep puncture wounds animal bites serious burns.

When using this product do not use in or near the eyes in case of contact, rinse eyes thoroughly with water do not apply over large areas of the body or in large quantities.

Stop use and ask a doctor if condition worsens irritation or rash appears and lasts for more than 72 hours.

Keep out of reach of children

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

Directions

For adults and Children two years and older: Apply the wipe thoroughly to the affected area. Use up to 3-4 times daily. For best results, allow the area to remain wet for 1-2 minutes.

Inactive Ingredients

Benzalkonium Chloride, Caprylyl Glycol, Phenoxyethanol, Polysorbate 20, Water.

Principal Display Panel

NUMB

FAST-ACTING

PAIN RELIEVING WIPE

LIDOCAINE INFUSED

Wipe Outz

1 X-LARGE WIPE (8 X 7 IN)

DO NOT FLUSH

INGREDIENTS AND APPEARANCE

LIDOCAINE TATTOO WIPE 
lidocaine hydrochloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85055-397
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE HYDROCHLORIDE ANHYDROUS	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85055-397-01	3 g in 1 PACKAGE; Type 0: Not a Combination Product	06/05/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	06/05/2025

Labeler - MD Tattoo Company (028607470)

Registrant - Diamond Wipes International, Inc. (161104729)

Establishment
Name	Address	ID/FEI	Business Operations
Diamond Wipes International, Inc.		161104729	manufacture(85055-397)