- Product NDC
- 57955-0041
- 11-digit product format
- 579550041
- Labeler code
- 57955
- Product ID
- 57955-0041_9feaa4d6-265a-4414-b288-b105c69870e0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antimonium tartaricum, Asterias rubens, Ferrum metallicum, Hepar sulphuris calcareum, Kali bromatum, Natrum muriaticum, Sanguinaria canadensis, Selenium metallicum, Sepia, Silica, Sulphur, Thuja occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- King Bio Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-05-21
- Marketing end
- 0000-00-00
- Substance
- ANTIMONY POTASSIUM TARTRATE; ASTERIAS RUBENS; IRON; CALCIUM SULFIDE; POTASSIUM BROMIDE; SODIUM CHLORIDE; SANGUINARIA CANADENSIS ROOT; SELENIUM; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG
- 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
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record