DERMATOME STAT

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
DERMATOME STAT
Generic name
ASTRAGALUS MEMBRANACEUS, ECHINACEA (ANGUSTIFOLIA), HYPERICUM PERFORATUM, HYDRASTIS CANADENSIS, DULCAMARA, GELSEMIUM SEMPERVIRENS, NITRICUM ACIDUM, RANUNCULUS BULBOSUS, THUJA OCCIDENTALIS
Manufacturer
Energique, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
6e48c2a9-f08a-418f-9b25-03a2010c340f
SPL ID
4bc06485-b85c-4da9-bc84-abf77bc23f18
Version
2
Effective date
2024-08-20
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:07:27
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: Stop use and ask a doctor if symptoms persist for more than 3 days. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. DO NOT UE IF TAMPER EVIDENT SEAL IS BROKEN OR MISSING Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.