- Product NDC
- 66579-0010
- 11-digit product format
- 665790010
- Labeler code
- 66579
- Product ID
- 66579-0010_3563d170-e38f-4916-816d-304fe5b78073
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antimonium tartaricum, Asterias rubens, Ferrum metallicum, Hepar sulphuris calcareum, Kali bromatum, Natrum muriaticum, Sanguinaria canadensis, Selenium metallicum, Sepia, Silicea, Sulphur, thuja occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- New Sun Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2010-07-21
- 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