Traumeel
- Product NDC
- 50114-7004
- 11-digit product format
- 501147004
- Labeler code
- 50114
- Product ID
- 50114-7004_11e7b387-3044-4f7f-b3e7-2938cae3d0b2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ARNICA MONTANA ROOT, ATROPA BELLADONNA, CALENDULA OFFICINALIS FLOWERING TOP, MATRICARIA RECUTITA, ACHILLEA MILLEFOLIUM, CALCIUM SULFIDE, COMFREY ROOT, ACONITUM NAPELLUS, BELLIS PERENNIS, MERCURIUS SOLUBILIS, HYPERICUM PERFORATUM, ECHINACEA, UNSPECIFIED, ECHINACEA PURPUREA and HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
- Dosage form
- INJECTION
- Route
- INTRA-ARTICULAR; INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Medinatura
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2007-05-09
- Marketing end
- 2024-12-31
- Substance
- ARNICA MONTANA ROOT; ATROPA BELLADONNA; CALENDULA OFFICINALIS FLOWERING TOP; MATRICARIA RECUTITA; ACHILLEA MILLEFOLIUM; CALCIUM SULFIDE; COMFREY ROOT; ACONITUM NAPELLUS; BELLIS PERENNIS; MERCURIUS SOLUBILIS; HYPERICUM PERFORATUM; ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
- Active strength
- 2 [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL; [hp_X]/2.2mL
- 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 |
|---|
| 50114-7004-1 | 50114700401 | 10 AMPULE in 1 CARTON (50114-7004-1) > 2.2 mL in 1 AMPULE | 10 ampule | 2007-05-09 | 2024-12-31 | No | No | Current |
| 50114-7004-2 | 50114700402 | 3 AMPULE in 1 CARTON (50114-7004-2) > 2.2 mL in 1 AMPULE | 3 ampule | 2007-05-09 | 2024-12-31 | No | No | Current |