Doctor Hoys Arnica Boost Recovery

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
Doctor Hoys Arnica Boost Recovery
Generic name
ARNICA MONTANA
Manufacturer
Dynamic Blending Specialists, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
7e639152-b423-4db8-9078-b5c929d6a07d
SPL ID
4769bbc4-c164-6de3-e063-6294a90a225f
Version
3
Effective date
2026-01-02
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:20:23
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 • Use as directed • Avoid contact with eyes Keep Out of reach of children If swallowed, get medical help or contact a Poison Control Center immediately If pregnant or breast feeding, • ask a health professional before use • Discontinue use of this product and consult a physician if condition worsens, or if symptoms persist for more than 7 days.

Reported adverse events (FAERS/openFDA)#

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