Home FDA labels 31103d8c-5ee4-483e-bd45-aac9eda84b68 Estrogen and Progesterone 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 Estrogen and Progesterone
Generic name AGNUS CASTUS, ANGELICA SINENSIS, APIS MELLIFICA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, ESTRADIOL, ESTRIOL, FOLLICULINUM, GALIUM APARINE, GLYCYRRHIZA GLABRA, KOREAN GINSENG, OOPHORINUM (SUIS), PROGESTERONE, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUM
Manufacturer ProBLEN
Product type HUMAN OTC DRUG
SPL set ID 71fec93b-43b7-4ebb-ab5c-5f544d8e6cbf
SPL ID 31103d8c-5ee4-483e-bd45-aac9eda84b68
Version 1
Effective date 2017-01-12
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:24 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Estrogen and Progesterone openfda.brand_name generic name AGNUS CASTUS, ANGELICA SINENSIS, APIS MELLIFICA, ARNICA MONTANA, CIMICIFUGA RACEMOSA, ESTRADIOL, ESTRIOL, FOLLICULINUM, GALIUM APARINE, GLYCYRRHIZA GLABRA, KOREAN GINSENG, OOPHORINUM (SUIS), PROGESTERONE, SEPIA, THUJA OCCIDENTALIS, VISCUM ALBUM openfda.generic_name manufacturer name ProBLEN openfda.manufacturer_name ndc package 43853-0017-1 openfda.package_ndc ndc package 43853-0017-2 openfda.package_ndc ndc product 43853-0017 openfda.product_ndc ndc11 package 43853001702 derived:openfda.package_ndc ndc11 package 43853001701 derived:openfda.package_ndc spl id 31103d8c-5ee4-483e-bd45-aac9eda84b68 id spl set id 71fec93b-43b7-4ebb-ab5c-5f544d8e6cbf set_id unii 2788Z9758H openfda.unii unii O80TY208ZW openfda.unii unii CUQ3A77YXI openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii S7YTV04R8O openfda.unii unii 4TI98Z838E openfda.unii unii 2DI9HA706A openfda.unii unii 433OSF3U8A openfda.unii unii B66F4574UG openfda.unii unii BK9092J5MP openfda.unii unii 4G7DS2Q64Y openfda.unii unii 7S82P3R43Z openfda.unii unii Z4B6561488 openfda.unii unii FB33469R8E openfda.unii unii K73E24S6X9 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: Not for use on children. If symptoms continue to recur, or if sleeplessness persists continuously for more than two weeks, consult a physician. Insomnia may be a symptom of a serious underlying medical illness. As with all medicines, if you are pregnant or breast feeding, consult a health professional before using this product. Keep out of the reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Tamper Evident. There is a seal around the neck of the bottle. Do not use if this seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.