- Product NDC
- 60512-9059
- 11-digit product format
- 605129059
- Labeler code
- 60512
- Product ID
- 60512-9059_c7c9c1f3-e944-487e-b2ef-fa51d9335e13
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AESCULUS HIPPOCASTANUM, HAMAMELIS VIRGINIANA, PAEONIA OFFICINALIS, COLLINSONIA, TEUCRIUM MARUM, VERBASCUM, BOLDO, SULPHUR, SODIUM NITRATE, RATANHIA, ACIDUM NITRICUM, NATRUM MURIATICUM, PODOPHYLLUM PELTATUM, RUTA GRAVEOLENS, APIS MELLIFICA
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-10-18
- Marketing end
- 0000-00-00
- Substance
- HORSE CHESTNUT; WITCH HAZEL; PAEONIA OFFICINALIS ROOT; COLLINSONIA CANADENSIS ROOT; TEUCRIUM MARUM; VERBASCUM THAPSUS; PEUMUS BOLDUS LEAF; SULFUR; SODIUM NITRATE; KRAMERIA LAPPACEA ROOT; NITRIC ACID; SODIUM CHLORIDE; PODOPHYLLUM PELTATUM ROOT; RUTA GRAVEOLENS FLOWERING TOP; APIS MELLIFERA
- Active strength
- 1 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record