- Product NDC
- 43742-2243
- 11-digit product format
- 437422243
- Labeler code
- 43742
- Product ID
- 43742-2243_9c99e905-07cd-41c8-887d-d8e0ae04c751
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Calendula Officinalis, Hamamelis Virginiana, Echinacea Purpurea, Bellis Perennis, Chamomilla, Hypericum Perforatum, Millefolium, Ledum Palustre, Arnica Montana, Bryonia (Alba), Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Symphytum Officinale, Rhus Tox, Aconitum Napellus, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Sulphuris Calcareum
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2025-01-14
- Substance
- ACHILLEA MILLEFOLIUM WHOLE; ACONITUM NAPELLUS WHOLE; ARNICA MONTANA WHOLE; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; COMFREY ROOT; ECHINACEA ANGUSTIFOLIA WHOLE; ECHINACEA PURPUREA WHOLE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM WHOLE; LACTIC ACID, L-; MATRICARIA CHAMOMILLA WHOLE; NADIDE; PANTOTHENIC ACID; RHODODENDRON TOMENTOSUM LEAFY TWIG; SUS SCROFA ADRENAL GLAND; SUS SCROFA UMBILICAL CORD; TOXICODENDRON PUBESCENS LEAF
- Active strength
- 3; 12; 4; 2; 8; 30; 1; 8; 1; 2; 1; 3; 8; 3; 8; 8; 4; 12; 12; 8 [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g; [hp_X]/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes