- Product NDC
- 60512-0007
- 11-digit product format
- 605120007
- Labeler code
- 60512
- Product ID
- 60512-0007_0653326e-43f6-4a4f-889a-218e05afe37d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SAPONARIA, ECHINACEA ANGUSTIFOLIA, KALIUM BROMATUM, VIOLA TRICOLOR, SELENIUM METALLICUM, NUX VOMICA, THUJA OCCIDENTALIS, PULSATILLA, CALCAREA PICRATA, SULPHUR IODATUM, ANTIMONIUM TARTARICUM
- Dosage form
- PELLET
- Route
- ORAL
- Labeler
- HOMEOLAB USA INC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2013-10-18
- Marketing end
- 0000-00-00
- Substance
- SAPONARIA OFFICINALIS ROOT; ECHINACEA ANGUSTIFOLIA; POTASSIUM BROMIDE; VIOLA TRICOLOR; SELENIUM; STRYCHNOS NUX-VOMICA SEED; THUJA OCCIDENTALIS LEAFY TWIG; PULSATILLA VULGARIS; CALCIUM PICRATE; SULFUR IODIDE; ANTIMONY POTASSIUM TARTRATE
- Active strength
- 3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record