Zeel
- Product NDC
- 50114-7030
- 11-digit product format
- 501147030
- Labeler code
- 50114
- Product ID
- 50114-7030_481ac8c7-8ec2-40e1-b29a-e846a24ad4a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ARNICA MONTANA ROOT, TOXICODENDRON PUBESCENS LEAF, SOLANUM DULCAMARA TOP, COMFREY ROOT, SULFUR, SANGUINARIA CANADENSIS ROOT, SUS SCROFA CARTILAGE, SUS SCROFA EMBRYO, SUS SCROFA UMBILICAL CORD, SUS SCROFA PLACENTA, .ALPHA.-LIPOIC ACID, COENZYME A, NADIDE and SODIUM DIETHYL OXALACETATE
- Dosage form
- INJECTION
- Route
- INTRA-ARTICULAR; INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- MediNatura
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-07-31
- Marketing end
- 2024-12-31
- Substance
- ARNICA MONTANA ROOT; TOXICODENDRON PUBESCENS LEAF; SOLANUM DULCAMARA TOP; COMFREY ROOT; SULFUR; SANGUINARIA CANADENSIS ROOT; SUS SCROFA CARTILAGE; SUS SCROFA EMBRYO; SUS SCROFA UMBILICAL CORD; SUS SCROFA PLACENTA; .ALPHA.-LIPOIC ACID; COENZYME A; NADIDE; SODIUM DIETHYL OXALACETATE
- Active strength
- 4 [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/2mL; [hp_X]/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 |
|---|
| 50114-7030-1 | 50114703001 | 10 AMPULE in 1 CARTON (50114-7030-1) > 2 mL in 1 AMPULE | 10 ampule | 2014-07-31 | 2024-12-31 | No | No | Current |
| 50114-7030-2 | 50114703002 | 3 AMPULE in 1 CARTON (50114-7030-2) > 2 mL in 1 AMPULE | 3 ampule | 2014-07-31 | 2024-12-31 | No | No | Current |