Osteoplex
- Product NDC
- 43857-0286
- 11-digit product format
- 438570286
- Labeler code
- 43857
- Product ID
- 43857-0286_609df051-e8e0-4dbd-9ca1-f035546a9fe7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- not applicable
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- BioActive Nutritional, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-08-22
- Marketing end
- 2020-08-26
- Substance
- EQUISETUM HYEMALE; MAGNESIUM CHLORIDE; COMFREY ROOT; ASCORBIC ACID; MANGANESE CHLORIDE; SUS SCROFA BONE MARROW; CALCIUM FLUORIDE; TRIBASIC CALCIUM PHOSPHATE; SILICON DIOXIDE; SUS SCROFA LIGAMENT; SUS SCROFA PARATHYROID GLAND
- Active strength
- 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record