BLACK COBRA TATTOO NUMBINGSPRAY 4% LIDOCAINE- lidocaine liquid

Black Cobra Tattoo NumbingSpray 4% Lidocaine by

Drug Labeling and Warnings

Black Cobra Tattoo NumbingSpray 4% Lidocaine by is a Otc medication manufactured, distributed, or labeled by Foshan Sugar Max Cosmetics CO.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Lidocaine 4%

PURPOSE

External Analgesic

INDICATIONS & USAGE

Temporarily relieves pain and itching due to: Tattoo procedures,
Minor scrapes, Minor cuts, Minor skin irritations,
Tattoo Laser Remova

WARNINGS

For external use only

WHEN USING

Keep out of reach of children.
Not foruse on children under 12 years old, consult a doctor beforeuse.
Avoid contact with eyes, mouth, or open wounds.
Do not apply over large areas of the body.

STOP USE

Stop use and seek medicaattention if irritation, rash, or an allergic reaction occurs, or ifsymptoms worsen or persist for more than seven days.

KEEP OUT OF REACH OF CHILDREN

lf swallowed, get medical help or contact Poison Control at 1-800-222-1222.Store at room temperature and do not freeze

DOSAGE & ADMINISTRATION

Adults and children 12 years and older: Apply a generouslayerto the affected area 15-30 minutes before the procedure.Allow the anesthetic to take effect, For prolonged comfort,reapply as necessary, but do not exceed 3 applications in 24hours. Children under 12 years: Consult a doctor before use.

INACTIVE INGREDIENT

Aqua
Propylene Glycol
Sodium Hyaluronate
Kojic Acid
Sodium Hydroxide
Trisodium Citrate
1,3-Butanediol
Phenoxyethanol
Ethylhexylglycerin

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BLACK COBRA TATTOO NUMBINGSPRAY 4% LIDOCAINE 
lidocaine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84938-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987)	LIDOCAINE	0.04 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
AQUA (UNII: 059QF0KO0R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
KOJIC ACID (UNII: 6K23F1TT52)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
TRISODIUM CITRATE (UNII: 1Q73Q2JULR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84938-003-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/26/2025

Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Sugar Max Cosmetics CO.,Ltd		700689935	manufacture(84938-003)