- Product NDC
- 50181-0005
- 11-digit product format
- 501810005
- Labeler code
- 50181
- Product ID
- 50181-0005_1ee48ddd-d7b6-4543-8cc7-26bfbedd9971
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DNA, Hypothalamus Suis, RNA, Sabal Serrulata, Glandula Suprarenalis Suis, Hydrocortisone (Cortisol), Hypophysis Suis, Testosterone, Chelidonium Majus, Thuja Occidentalis
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- The Wellness Center for Research and Education, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-10-11
- Marketing end
- 0000-00-00
- Substance
- HERRING SPERM DNA; SUS SCROFA HYPOTHALAMUS; SACCHAROMYCES CEREVISIAE RNA; SAW PALMETTO; HYDROCORTISONE; SUS SCROFA ADRENAL GLAND; SUS SCROFA PITUITARY GLAND; TESTOSTERONE; CHELIDONIUM MAJUS; THUJA OCCIDENTALIS LEAFY TWIG
- Active strength
- 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record