Arnica Treatment Pack

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
Arnica Treatment Pack
Generic name
ARNICA TREATMENT PACK
Manufacturer
Nartex Laboratorios Homeopaticos SA DE CV
Product type
HUMAN OTC DRUG
SPL set ID
86431a9a-5b53-c28a-e053-2991aa0a9901
SPL ID
86431a9a-5b54-c28a-e053-2991aa0a9901
Version
1
Effective date
2019-04-11
Source export date
2026-11-06
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/2026-11-06/3744b3ae389d13e8f30cade845ea29e0fc75bb043dcda980c2025693f0c10522/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 09:10:43
Harmonized routes table
Harmonized routes
ORAL, TOPICAL

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings Do not use if you have an allergy or hypersensitivity to the components of the fourmal or have had a prior reaction to this product.

warnings

Warnings For external use only. Do not Apply to wounds tor damaged skin apply over large areas of the body

Reported adverse events (FAERS/openFDA)#

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