DE LA CRUZ GENTIAN VIOLET- gentian violet tincture

DE LA CRUZ GENTIAN VIOLET by

Drug Labeling and Warnings

DE LA CRUZ GENTIAN VIOLET by is a Otc medication manufactured, distributed, or labeled by DLC Laboratories, Inc., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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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

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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)

INGREDIENTS AND APPEARANCE

DE LA CRUZ GENTIAN VIOLET 
gentian violet tincture

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 24286-1531
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GENTIAN VIOLET (UNII: J4Z741D6O5) (GENTIAN VIOLET CATION - UNII:3GVJ31T6YY)	GENTIAN VIOLET	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)	10 mL  in 100 mL
WATER (UNII: 059QF0KO0R)

Product Characteristics
Color	purple	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 24286-1531-7	30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	12/13/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/23/2017

Labeler - DLC Laboratories, Inc. (093351930)

Registrant - Humco Holding Group, inc. (825672884)