Home NDC 43742-1518 Hormone Combination
Product NDC 43742-1518
11-digit product format 437421518
Labeler code 43742
Product ID 43742-1518_fea3c464-8d7e-46db-b159-a305956a8618
Type HUMAN OTC DRUG
Nonproprietary name Acetaldehyde, Dopamine Hydrochloride, DHEA (Dehydroepiandrosterone), 7-Oxo- Dehydroepiandrosterone 3-Acetate, Folliculinum, Oophorinum (Suis), Cholesterinum, Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-08-21
Substance 7-KETO-DEHYDROEPIANDROSTERONE; ACETALDEHYDE; ALDOSTERONE; ANDROSTERONE; CHOLESTEROL; CORTISONE ACETATE; DOPAMINE HYDROCHLORIDE; ESTRONE; FOLLITROPIN; PRASTERONE; PROGESTERONE; SUS SCROFA OVARY; TESTOSTERONE
Active strength 6; 6; 12; 12; 8; 12; 6; 8; 12; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Catecholamine [EPC], Catecholamines [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Gonadotropin [EPC], Gonadotropins [CS], Progesterone [CS], Progesterone [EPC]
DEA schedule CIII
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Hormone Combination
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETALDEHYDE 6 [hp_X]/mL DOPAMINE HYDROCHLORIDE 6 [hp_X]/mL PRASTERONE 12 [hp_C]/mL 7-KETO-DEHYDROEPIANDROSTERONE 12 [hp_C]/mL ESTRONE 8 [hp_X]/mL SUS SCROFA OVARY 12 [hp_X]/mL CHOLESTEROL 6 [hp_X]/mL PROGESTERONE 8 [hp_X]/mL TESTOSTERONE 12 [hp_C]/mL CORTISONE ACETATE 6 [hp_X]/mL ALDOSTERONE 8 [hp_X]/mL ANDROSTERONE 8 [hp_X]/mL FOLLITROPIN 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-1518-1 Hormone Combination 30 mL in 1 BOTTLE, DROPPER LIQUID 30 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1518 HORMONE COMBINATION (ACETALDEHYDE, DOPAMINE HYDROCHLORIDE, DHEA (DEHYDROEPIANDROSTERONE), 7-OXO- DEHYDROEPIANDROSTERONE 3-ACETATE, FOLLICULINUM, OOPHORINUM (SUIS), CHOLESTERINUM, PROGESTERONE, TESTOSTERONE, CORTISONE ACETICUM, ALDOSTERONE, ANDROSTERONE, FOLLICLE STIMULATING HORMONE) LIQUID [DESERET BIOLOGICALS, INC.] 6 Current NDC, Legacy NDC, 1 package rows 20240312_22908e3d-492c-4b18-a070-076f99a81314.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Hormone Combination ACETALDEHYDE, DOPAMINE HYDROCHLORIDE, DHEA (DEHYDROEPIANDROSTERONE), 7-OXO- DEHYDROEPIANDROSTERONE 3-ACETATE, FOLLICULINUM, OOPHORINUM (SUIS), CHOLESTERINUM, PROGESTERONE, TESTOSTERONE, CORTISONE ACETICUM, ALDOSTERONE, ANDROSTERONE, FOLLICLE STIMULATING HORMONE Deseret Biologicals, Inc. 22908e3d-492c-4b18-a070-076f99a81314 2024-03-11 Warnings Exact identifier ndc (product): 43742-1518
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1518-1 43742151801 30 mL in 1 BOTTLE, DROPPER (43742-1518-1) 30 ml 2019-08-21 0000-00-00 No No Current