FDA.reportPublic FDA data

DE LA CRUZ GENTIAN VIOLET

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
DE LA CRUZ GENTIAN VIOLET
Generic name
GENTIAN VIOLET
Manufacturer
DLC Laboratories, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
d7b4ca59-1bc3-4540-bc0a-2f4b7495a0a7
SPL ID
2a80c1ae-e663-ab81-e063-6394a90ab73c
Version
9
Effective date
2024-12-30
Source export date
2026-08-01
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/8ac060fefb6f4d67c41cc2c9e4330286ca93c48094c18386c11bf706a1d8bd34/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:29:18
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

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.