ActivMend Pro
ActivMend Pro is an FDA drug label for the active ingredient ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS manufactured by Cearna, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230110.
- Generic name
- ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS
- Manufacturer
- Cearna, Inc.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 76277-123
- Application
- N/A
- Label effective
- 20230110
About this product
ActivMend Pro is an FDA-registered drug product whose active ingredient is ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS. It is labelled by Cearna, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 76277-123, label effective 20230110. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, RHUS TOXICODENDRON, RUTA GRAVEOLENS are most often described in connection with: reduction swelling, pain associated, joint sprains, muscle strains, shin splints, dislocations overuse. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For the reduction of swelling and pain associated with joint sprains, muscle strains, shin splints, dislocations, overuse injuries, and bruising.
Dosage & Administration
Directions Directions: Adults and Children 12 years of age and over Clean and dry affected area. Remove patch from film. Place healing pads on intact skin. Wear one activMend patch up to 24 hours. Children under 12 years of age - Consult a doctor
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.
Frequently asked questions
What is ActivMend Pro used for?
Uses For the reduction of swelling and pain associated with joint sprains, muscle strains, shin splints, dislocations, overuse injuries, and bruising.
Who makes ActivMend Pro?
Cearna, Inc. is the labeler of record for ActivMend Pro.
What form does ActivMend Pro come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is ActivMend Pro prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has ActivMend Pro been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.