ActivMend Pro

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
ActivMend Pro
Generic name
ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS
Manufacturer
Cearna, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
baf1a1fe-dc23-d7ca-e053-2995a90ab4fb
SPL ID
f1eb77a2-687c-1cc4-e053-2a95a90a8009
Version
2
Effective date
2023-01-10
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 06:18:07
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 Warnings For external use on intact skin only Use only as directed. Do not bandage tightly. Stop use and ask a doctor if condition worsens. Do not use in the eyes, over open wounds, or if you have unexpected bleeding. If pregnant or breast-feeding, ask a health professional before use. Do not use if you are allergic to any of this product's active or ingredients.

Reported adverse events (FAERS/openFDA)#

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