Label: DE LA CRUZ GENTIAN VIOLET- gentian violet tincture
- NDC Code(s): 24286-1531-7, 24286-1531-8
- Packager: DLC Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 30, 2024
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Warnings
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
- Directions
- Other information
- Inactive ingredients
- Questions
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DE LA CRUZ GENTIAN VIOLET
gentian violet tinctureProduct 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 2 NDC:24286-1531-8 59 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 01/20/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 11/01/2012 Labeler - DLC Laboratories, Inc. (093351930) Registrant - Pharma Nobis, LLC (118564114)






