- Product NDC
- 50114-7041
- 11-digit product format
- 501147041
- Labeler code
- 50114
- Product ID
- 50114-7041_b56ceb53-f812-40b1-967e-72a85d653e62
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LACTIC ACID, L- and VISCUM ALBUM and COLCHICUM AUTUMNALE BULB and CONIUM MACULATUM FLOWERING TOP and GALIUM APARINE and FUCUS VESICULOSUS and SEDUM ACRE and SEMPERVIVUM TECTORUM LEAF and ADENOSINE TRI
- Dosage form
- INJECTION
- Route
- INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Heel Inc
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-07-08
- Marketing end
- 0000-00-00
- Substance
- LACTIC ACID, L-; COLCHICUM AUTUMNALE BULB; CONIUM MACULATUM FLOWERING TOP; GALIUM APARINE; FUCUS VESICULOSUS; SEDUM ACRE; SEMPERVIVUM TECTORUM LEAF; ADENOSINE TRIPHOSPHATE; FUMARIC ACID; .ALPHA.-KETOGLUTARIC ACID; MALIC ACID; SODIUM DIETHYL OXALACETATE; PULSATILLA VULGARIS; SPONGIA OFFICINALIS SKELETON, ROASTED; SUS SCROFA THYROID; CALCIUM FLUORIDE; SUS SCROFA UMBILICAL CORD; PORK LIVER; SUS SCROFA BONE MARROW; SUS SCROFA SPLEEN; SULFUR; SUS SCROFA THYMUS; VISCUM ALBUM FRUIT; CORTISONE ACETATE
- Active strength
- 3 [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; [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
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record