DE LA CRUZ GENTIAN VIOLET- gentian violet tincture 
DLC Laboratories, Inc.

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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 DrugM00311/01/2012
Labeler - DLC Laboratories, Inc. (093351930)
Registrant - Pharma Nobis, LLC (118564114)

Revised: 12/2024
Document Id: 2a80c1ae-e663-ab81-e063-6394a90ab73c
Set id: d7b4ca59-1bc3-4540-bc0a-2f4b7495a0a7
Version: 9
Effective Time: 20241230
 
DLC Laboratories, Inc.