Celeragesic
- Product NDC
- 43742-0847
- 11-digit product format
- 437420847
- Labeler code
- 43742
- Product ID
- 43742-0847_0a6e2bd3-aebf-4a6d-8cbe-4dfd95de3f87
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Echinacea (Angustifolia), Calendula Officinalis, Hamamelis Virginiana, Echinacea Purpurea, Bellis Perennis, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia (Alba), Arnica Montana, Rhus Tox, Adenosinum Triphosphoricum Dinatrum, Clematis Vitalba, Flos, Helianthemum Nummularium, Flos, Hepar Sulphuris Calcareum, Impatiens Glandulifera, Flos, Mercurius Solubilis, Nadidum, Ornithogalum Umbellatum, Flos, Pantothenic Acid, Prunus Cerasifera, Flos, Sarcolacticum Acidum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-09-15
- Marketing end
- 2021-12-20
- Substance
- ECHINACEA ANGUSTIFOLIA; CALENDULA OFFICINALIS FLOWERING TOP; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; ECHINACEA PURPUREA; BELLIS PERENNIS; ACONITUM NAPELLUS; MATRICARIA RECUTITA; HYPERICUM PERFORATUM; ATROPA BELLADONNA; ACHILLEA MILLEFOLIUM; BRYONIA ALBA ROOT; ARNICA MONTANA; TOXICODENDRON PUBESCENS LEAF; ADENOSINE TRIPHOSPHATE DISODIUM; CLEMATIS VITALBA FLOWER; HELIANTHEMUM NUMMULARIUM FLOWER; CALCIUM SULFIDE; IMPATIENS GLANDULIFERA FLOWER; MERCURIUS SOLUBILIS; NADIDE; ORNITHOGALUM UMBELLATUM FLOWERING TOP; PANTOTHENIC ACID; PRUNUS CERASIFERA FLOWER; LACTIC ACID, L-; COMFREY ROOT; UBIDECARENONE; ACTIVATED CHARCOAL; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS; PROTEUS MORGANII
- Active strength
- 1 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-0847-1 | 43742084701 | 30 mL in 1 BOTTLE, DROPPER (43742-0847-1) | 30 ml | 2016-09-15 | 2021-12-20 | No | No | Current |