ActivMend

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
Generic name: ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS, NATRUM MURATICUM
Manufacturer: Cearna, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: baefc5d4-a7e4-4ba2-e053-2995a90a4b86
SPL ID: 46a62102-1d75-11cb-e063-6394a90a9657
Version: 4
Effective date: 2025-12-23
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:34

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		ActivMend	openfda.brand_name
generic name		ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS, NATRUM MURATICUM	openfda.generic_name
manufacturer name		Cearna, Inc.	openfda.manufacturer_name
ndc	package	76277-122-32	openfda.package_ndc
ndc	product	76277-122	openfda.product_ndc
ndc11	package	76277012232	derived:openfda.package_ndc
spl id		46a62102-1d75-11cb-e063-6394a90a9657	id
spl set id		baefc5d4-a7e4-4ba2-e053-2995a90a4b86	set_id
unii		877L01IZ0P	openfda.unii
unii		XK4IUX8MNB	openfda.unii
unii		O80TY208ZW	openfda.unii
unii		N94C2U587S	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		6IO182RP7A	openfda.unii

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 on intact skin only Do not use if you are allergic to any of this product's active or inactive ingredients. When using this product use only as directed do not bandage tightly avoid contact with eyes do not apply to wounds or damaged skin Stop use and ask a doctor if condition worsens irritation occurs symptoms persist for more than 7 days or clear up and occur again within a few days I f pre gnant or breastfeeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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