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
2026-09-28
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/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:20:21
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.