DE LA CRUZ GENTIAN VIOLET- gentian violet tincture 
DLC Laboratories, 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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DE LA CRUZ ® GENTIAN VIOLET 1%

Drug Facts

Active ingredient

Gentian violet 1%

Purpose

Antiseptic

Uses

First aid to help prevent infection in minor:

Warnings

For external use only

Consult a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

  • do not use in or near the eyes or over large areas of the body
  • do not apply to an ulcerative lesion as this may result in tattooing of the skin

Stop use and consult a doctor if

  • redness, irritation, swelling or pain persists or increases, or if infection or rash occurs
  • symptoms persist for more than 7 days, or clear up and occur again within a few days

KEEP OUT OF THE REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Other information

Inactive ingredients

alcohol, purified water

Questions

1-800-858-3889

Manufactured by
DE LA CRUZ PRODUCTS
A DIVISION OF DLC LABORATORIES, INC.
PARAMOUNT, CA 90723 USA

PRINCIPAL DISPLAY PANEL

DLC GV 5-16-23DLC GV 1 2floz.jpgDLCGV.jpgSpanish

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DE LA CRUZ GENTIAN VIOLET 
gentian violet tincture
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1531
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GENTIAN VIOLET (UNII: J4Z741D6O5) (GENTIAN VIOLET CATION - UNII:3GVJ31T6YY) GENTIAN VIOLET1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M) 10 mL  in 100 mL
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorpurpleScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:24286-1531-730 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product12/13/2017
2NDC:24286-1531-859 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/20/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E11/01/2012
Labeler - DLC Laboratories, Inc. (093351930)
Registrant - Pharma Nobis, LLC (118564114)

Revised: 5/2023
Document Id: fbd11484-90b4-4562-e053-6294a90a10c6
Set id: d7b4ca59-1bc3-4540-bc0a-2f4b7495a0a7
Version: 8
Effective Time: 20230516
 
DLC Laboratories, Inc.