United States · FDA National Drug Code directory

Adrenal and DHEA

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
43853-0020_a808f440-abf4-4652-8ac6-f0dce3212a86
Product NDC
43853-0020
Form
LIQUID
Composition / generic term
Aralia Quinquefolia, Ashwagandha, Avena Sativa, Carduus Marianus, Dhea, Glandula Suprarenalis Suis, L-Arginine, Natrum Muriaticum, Phosphoricum Acidum, Rhodiola.
Labeler
ProBLEN
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start / end (source format)
20170509
Source listing expiry
20261231

Source-listed ingredients

  • AMERICAN GINSENG — 3 [hp_X]/30mL
  • WITHANIA SOMNIFERA ROOT — 3 [hp_X]/30mL
  • AVENA SATIVA FLOWERING TOP — 3 [hp_X]/30mL
  • MILK THISTLE — 3 [hp_X]/30mL
  • PRASTERONE — 6 [hp_X]/30mL
  • SUS SCROFA ADRENAL GLAND — 12 [hp_X]/30mL
  • ARGININE — 6 [hp_X]/30mL
  • SODIUM CHLORIDE — 30 [hp_C]/30mL
  • PHOSPHORIC ACID — 200 [hp_C]/30mL
  • RHODIOLA KIRILOWII ROOT — 3 [hp_X]/30mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 mL in 1 BOTTLE, SPRAY (43853-0020-1) · 43853-0020-1

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →