Home FDA labels fea3c464-8d7e-46db-b159-a305956a8618 Hormone Combination openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name Hormone Combination
Generic name ACETALDEHYDE, DOPAMINE HYDROCHLORIDE, DHEA (DEHYDROEPIANDROSTERONE), 7-OXO- DEHYDROEPIANDROSTERONE 3-ACETATE, FOLLICULINUM, OOPHORINUM (SUIS), CHOLESTERINUM, PROGESTERONE, TESTOSTERONE, CORTISONE ACETICUM, ALDOSTERONE, ANDROSTERONE, FOLLICLE STIMULATING HORMONE
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 22908e3d-492c-4b18-a070-076f99a81314
SPL ID fea3c464-8d7e-46db-b159-a305956a8618
Version 6
Effective date 2024-03-11
Source export date 2026-09-28
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:37:04 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Hormone Combination openfda.brand_name generic name ACETALDEHYDE, DOPAMINE HYDROCHLORIDE, DHEA (DEHYDROEPIANDROSTERONE), 7-OXO- DEHYDROEPIANDROSTERONE 3-ACETATE, FOLLICULINUM, OOPHORINUM (SUIS), CHOLESTERINUM, PROGESTERONE, TESTOSTERONE, CORTISONE ACETICUM, ALDOSTERONE, ANDROSTERONE, FOLLICLE STIMULATING HORMONE openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-1518-1 openfda.package_ndc ndc product 43742-1518 openfda.product_ndc ndc11 package 43742151801 derived:openfda.package_ndc spl id fea3c464-8d7e-46db-b159-a305956a8618 id spl set id 22908e3d-492c-4b18-a070-076f99a81314 set_id unii 4964P6T9RB openfda.unii unii 459AG36T1B openfda.unii unii GO1N1ZPR3B openfda.unii unii 883WKN7W8X openfda.unii unii 7L3E358N9L openfda.unii unii 2334LJD2E9 openfda.unii unii S7YTV04R8O openfda.unii unii 3XMK78S47O openfda.unii unii 97C5T2UQ7J openfda.unii unii 2DI9HA706A openfda.unii unii C24W7J5D5R openfda.unii unii 076WHW89TW openfda.unii unii 4G7DS2Q64Y openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.