LIDOCAINE- lidocaine liquid 
SUNFLORA, INC

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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73240-004-03

3oz

LIDOCAINE 
lidocaine liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73240-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE4 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
WATER (UNII: 059QF0KO0R)  
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
DIMETHICONE 1000 (UNII: MCU2324216)  
XANTHAN GUM (UNII: TTV12P4NEE)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73240-004-0385 g in 1 APPLICATOR; Type 0: Not a Combination Product01/26/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34801/26/2021
Labeler - SUNFLORA, INC (067153368)

Revised: 5/2022
Document Id: dfc2121b-1cec-3e4f-e053-2995a90a1909
Set id: b9cfcc8d-c3f4-d253-e053-2a95a90a31b3
Version: 9
Effective Time: 20220524
 
SUNFLORA, INC