DermaNumb Tattoo Anesthetic Spray

DermaNumb Tattoo Anesthetic by

Drug Labeling and Warnings

DermaNumb Tattoo Anesthetic by is a Otc medication manufactured, distributed, or labeled by A.T.S. Laboratories, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DERMANUMB TATTOO ANESTHETIC- lidocaine hcl gel 
A.T.S. Laboratories, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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DermaNumb Tattoo Anesthetic Spray

Active Ingredients

Lidocaine HCL 4.0% w/w

Purpose

External Analgesic

Uses

For temporary relief of pain and itching associated with minor cuts or minor skin irritations.

Warnings

​For external use only

Avoid contact with eyes

​Do not use ​in large quantities, particularly over raw surfaces or blistered areas

​Stop use and ask doctor if

​ Condition worsens, or if symptoms persist for more then 7 days or clear up and occur again with a few days.  Discontinue use.

​Keep out of reach of children

If product is swallowed, get medical help or contact a poison control center right away.

Directions

For adults and children two-years or older: Apply to affected area not more than 3 to 4 times daily.  Children under 2 years of age: consult a physician.

Inactive Ingredients

Achillea Millegolium (Yarrow) Extract, Caprylyl Glycol, Citric Acid, Disodium EDTA, Methylisothiazolinone, Propylene Glycol, Schidigera (Yucca) Root Extract, Sodium Metabisulfate, Water.

Other Information

Protect this product from excessive heat and direct sun.

Questions or Comments?

954-492-9898

1oz Label

4oz Label

DERMANUMB TATTOO ANESTHETIC 
lidocaine hcl gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 70188-001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)  
YUCCA SCHIDIGERA (UNII: 08A0YG3VIC)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 70188-001-0128 g in 1 PACKAGE; Type 0: Not a Combination Product07/01/201501/12/2018
2NDC: 70188-001-04113 g in 1 PACKAGE; Type 0: Not a Combination Product07/01/201501/12/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/01/201501/12/2018
Labeler - A.T.S. Laboratories, LLC (080013331)

Revised: 12/2019
 
A.T.S. Laboratories, LLC