- Product NDC
- 60986-2000
- 11-digit product format
- 609862000
- Labeler code
- 60986
- Product ID
- 60986-2000_1084b58e-310d-46c1-8a6c-0680132ba6e4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ECHINACEA ANGUSTIFOLIA, HAMAMMELIS VIRGINIANA, CALCAREA PHOSPHORICA, HYDRASTIS CANADANESIS, SENEGA OFFICINALIS, SILICEA, CONIUM, AURUM MURIATICUM NATRONATUM, CALCAREA CARBONICA, FUCUS VESICULOSUS, LAC
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Marco Pharma International LLC.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 1992-03-01
- Marketing end
- 0000-00-00
- Substance
- ECHINACEA ANGUSTIFOLIA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; TRIBASIC CALCIUM PHOSPHATE; GOLDENSEAL; POLYGALA SENEGA ROOT; SILICON DIOXIDE; CONIUM MACULATUM FLOWERING TOP; SODIUM TETRACHLOROAURATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; FUCUS VESICULOSUS; LACHESIS MUTA VENOM
- 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
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record