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DE LA CRUZ GENTIAN VIOLET

Dosage form: tincture
Ingredients: GENTIAN VIOLET 1g in 100mL
Labeler: DLC Laboratories, Inc.
NDC Code: 24286-1531

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.

DE LA CRUZ ® GENTIAN VIOLET 1%

Drug Facts

Active ingredient

Gentian violet 1%

Purpose

First aid antiseptic

Uses

First aid antiseptic to help prevent infection in minor:

  • cuts
  • scrapes
  • burns

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
  • 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

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions
  • clean the affected area
  • apply a small amount of this product to the area 1 to 2 times daily
  • do not bandage

Other information
  • will stain skin and clothing

Inactive ingredients

alcohol, purified water

Questions

1-800-858-3889

Distributed by:
De La Cruz Products
A Division of DLC Laboratories, Inc.
Paramount, CA 90723 USA

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Label

De La Cruz ®

Gentian Violet

1% Sol. • Alcohol 10%

First Aid Antiseptic

TRUSTED
QUALITY

For External Use Only

1 FL OZ
(30 mL)

DE LA CRUZ GENTIAN VIOLET 
gentian violet tincture
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24286-1531
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GENTIAN VIOLET (GENTIAN VIOLET CATION) GENTIAN VIOLET1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL10 mL  in 100 mL
WATER 
Product Characteristics
ColorpurpleScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:24286-1531-730 mL in 1 BOTTLE, WITH APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E08/23/2017
Labeler - DLC Laboratories, Inc. (093351930)
Registrant - Humco Holding Group, inc. (825672884)

 
DLC Laboratories, Inc.

Medically reviewed on Jul 17, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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