Traumeel Rx
- Product NDC
- 51885-9482
- 11-digit product format
- 518859482
- Labeler code
- 51885
- Product ID
- 51885-9482_db6cafe0-6015-4e1e-9285-c5b84b623055
- 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
- Biologische Heilmittel Heel
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51885-9482-6 | 51885948206 | 4 g in 1 TUBE (51885-9482-6) | 4 g | 2016-04-28 | 0000-00-00 | No | No | Current |
| 51885-9482-8 | 51885948208 | 1 TUBE in 1 CARTON (51885-9482-8) > 100 g in 1 TUBE | 1 tube | 2016-04-28 | 0000-00-00 | No | No | Current |