TATTOO NUMBING CREAM- lidocaine cream

Tattoo numbing cream by

Drug Labeling and Warnings

Tattoo numbing cream by is a Otc medication manufactured, distributed, or labeled by Haikou Pucao Trading Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

lidocaine 5%

PURPOSE

local anesthetic

INDICATIONS & USAGE

For the temporary alleviation of localized discomfort, pruritus, pain, or burning sensation in the perianal area associated with anorectal disorders.

WARNINGS

For external use only

• an allergic reaction occurs.
• symptom does not improve or if redness, irritation, swelling, pain or other symptoms develop or increase.

do not exceed the recommended daily dosage unless directed by a doctor. Avoid inserting this product into the rectum using fingers, medical devices, or applicators. Do not use if you are allergic to the ingredients in this product of if the seal is broken or missing.

ask a health professional before use.

in case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

For children under 12, consult a doctor.
For adults: If possible, clean the affected area with mild soap and warm water, making sure to rinse thoroughly. Gently dry the area with toilet tissue or a soft colth before applying the product.
Apply up to 4 times daily.

OTHER SAFETY INFORMATION

• store room temperature 59º-86ºF (15º-30ºC)
• keep away from direct sunlight or heat

INACTIVE INGREDIENT

Carbomer 934, Lecithin(Soybean), Emu Oil, Arnica, Propylene Glycol, Tocopheryl Acetate, Benzyl Alcohol, Aqua.

QUESTIONS

contact us at service@nupharco.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TATTOO NUMBING CREAM 
lidocaine cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85261-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER 934 (UNII: Z135WT9208)
BENZYL ALCOHOL (UNII: LKG8494WBH)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
EMU OIL (UNII: 344821WD61)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85261-101-01	60 mL in 1 TUBE; Type 0: Not a Combination Product	04/25/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/25/2025

Labeler - Haikou Pucao Trading Co.,Ltd (621948245)