- Product NDC
- 57955-0115
- 11-digit product format
- 579550115
- Labeler code
- 57955
- Product ID
- 57955-0115_62ad50d4-ff03-4732-bf13-1c5374f0c150
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Agnus castus, Aletris farinosa, Berberis vulgaris, Caulophyllum thalictroides, Ferrum metallicum, Graphites, Helonias dioica, Ignatia amara, Lilium tigrinum, Lycopodium clavatum, Natrum muriaticum, Onosmodium virginianum, Pulsatilla, Sepia
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-18
- Marketing end
- 0000-00-00
- Substance
- CHASTE TREE; ALETRIS FARINOSA ROOT; BERBERIS VULGARIS ROOT BARK; CAULOPHYLLUM THALICTROIDES ROOT; IRON; GRAPHITE; CHAMAELIRIUM LUTEUM ROOT; STRYCHNOS IGNATII SEED; LILIUM LANCIFOLIUM WHOLE FLOWERING; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; ONOSMODIUM VIRGINIANUM WHOLE; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE
- Active strength
- 10 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record