Adrenal Support
- Product NDC
- 43742-0197
- 11-digit product format
- 437420197
- Labeler code
- 43742
- Product ID
- 43742-0197_caff8ad0-b723-446e-aaf7-9637b8deb07d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aralia Quinquefolia, Humulus Lupulus, Adrenalinum, Cortisone Aceticum, Thyroidinum (Suis), Selenium Metallicum, Arsenicum Album, Calcarea Carbonica, Convallaria Majalis, Crotalus Horridus, Ferrum Metallicum, Nux Vomica, Phosphorus, Sepia, Phosphoricum Acidum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2012-11-14
- Marketing end
- 2020-11-06
- Substance
- AMERICAN GINSENG; HOPS; EPINEPHRINE; CORTISONE ACETATE; SUS SCROFA THYROID; SELENIUM; ARSENIC TRIOXIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CONVALLARIA MAJALIS; CROTALUS HORRIDUS HORRIDUS VENOM; IRON; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS; SEPIA OFFICINALIS JUICE; PHOSPHORIC ACID
- 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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record