84938-003 Black Cobra Tattoo Numbing Spray 4% Lidocaine

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]

BLACK COBRA TATTOO NUMBINGSPRAY 4% LIDOCAINE- lidocaine liquid 
Foshan Sugar Max Cosmetics CO.,Ltd

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84938-003 Black Cobra Tattoo Numbing Spray 4% Lidocaine

Lidocaine 4%

External Analgesic


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

For external use only


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

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

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.

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

label2

BLACK COBRA TATTOO NUMBINGSPRAY 4% LIDOCAINE 
lidocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 84938-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE0.04 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
TRISODIUM CITRATE (UNII: 1Q73Q2JULR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 84938-003-0130 mL in 1 BOTTLE; Type 0: Not a Combination Product05/26/202507/24/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01705/26/202507/24/2025
Labeler - Foshan Sugar Max Cosmetics CO.,Ltd (700689935)
Establishment
NameAddressID/FEIBusiness Operations
Foshan Sugar Max Cosmetics CO.,Ltd700689935manufacture(84938-003)

Revised: 7/2025