Traumeel Rx
- Product NDC
- 50114-9482
- 11-digit product format
- 501149482
- Labeler code
- 50114
- Product ID
- 50114-9482_08b99591-f7a1-42b4-a356-3bdd01a4755a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ACONITUM NAPELLUS, ARNICA MONTANA ROOT, ATROPA BELLADONNA, BELLIS PERENNIS, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ECHINACEA, UNSPECIFIED, ECHINACEA PURPUREA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, CALCIUM SULFIDE, HYPERICUM PERFORATUM, MERCURIUS SOLUBILIS, ACHILLEA MILLEFOLIUM and COMFREY ROOT
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- MediNatura Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-04-28
- Marketing end
- 2023-10-31
- Substance
- ACONITUM NAPELLUS; ARNICA MONTANA ROOT; ATROPA BELLADONNA; BELLIS PERENNIS; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; CALCIUM SULFIDE; HYPERICUM PERFORATUM; MERCURIUS SOLUBILIS; ACHILLEA MILLEFOLIUM; COMFREY ROOT
- Active strength
- 1 [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
- 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 |
|---|
| 50114-9482-3 | 50114948203 | 4 g in 1 POUCH (50114-9482-3) | 4 g | 2016-04-28 | 2023-10-31 | No | No | Current |
| 50114-9482-8 | 50114948208 | 1 TUBE in 1 CARTON (50114-9482-8) > 100 g in 1 TUBE | 1 tube | 2016-04-28 | 2023-10-31 | No | No | Current |