DRAGON PAIN NUMBING ROLL-ON- lidocaine hydrochloride liquid 
Genomma Lab USA

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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Dragon® Pain Numbing Roll-On

Drug Facts

Active ingredient

Lidocaine HCl 4%

Purpose

Topical analgesic

Use

Warnings

For external use only

Do not use

  • on large areas of the body, particularly over raw surfaces or blistered areas
  • on wounds or damaged skin

When using this product

  • use only as directed
  • avoid contact with eyes
  • do not apply tight bandages
  • do not apply a heating pad to treated skin
  • do not use in large quantities

Stop use and ask a doctor if

  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children to avoid accidental ingestion. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients

Acrylates / C10-30 Alkyl Acrylate Crosspolymer, Alcohol Denat., Aminomethyl Propanol, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Caprylyl Methicone, Cetearyl Alcohol, Ceteth-20 Phosphate, Decolorized Aloe Barbadensis Leaf Juice, Dicetyl Phosphate, Dimethicone, Disodium EDTA, Ethylhexylglycerin, Glyceryl StearateSE, Phenoxyethanol, Steareth-21, Water

Questions or comments?

Call toll free 1-877-994-3666

Distributed by
Genomma Lab USA, Inc.,
Houston, TX 77027

PRINCIPAL DISPLAY PANEL - 71 g Container Carton

POMADA
DRAGON®

Lidocaine HCl 4%

PAIN NUMBING ROLL ON

MAX STRENGTH

NUMBS PAIN
FAST

HOURS OF
RELIEF

ODOR
FREE

KEEPS HANDS CLEAN!

BLOCKS PAIN
RECEPTORS

NO MESS
APPLICATOR!

NET WT 2.5 oz (71 g)

PRINCIPAL DISPLAY PANEL - 71 g Container Carton
DRAGON PAIN NUMBING ROLL-ON 
lidocaine hydrochloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50066-411
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Lidocaine hydrochloride (UNII: V13007Z41A) (LIDOCAINE - UNII:98PI200987) LIDOCAINE HYDROCHLORIDE ANHYDROUS40 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Alcohol (UNII: 3K9958V90M)  
Water (UNII: 059QF0KO0R)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
ceteth-20 phosphate (UNII: 921FTA1500)  
Steareth-21 (UNII: 53J3F32P58)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50066-411-021 in 1 CARTON07/24/2021
171 g in 1 CONTAINER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34807/24/2021
Labeler - Genomma Lab USA (832323534)

Revised: 7/2021
Document Id: 45415c6f-3939-47fd-85c9-705fe1c36734
Set id: 65cbdda6-b555-49fb-86e7-ce458c64cae0
Version: 1
Effective Time: 20210726
 
Genomma Lab USA