Home FDA labels 4e326cd0-c586-4d82-80ef-0ae5dd294dcc Hypothaltem 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 Hypothaltem
Generic name EUPATORIUM PERFOLIATUM, BERBERIS VULGARIS, MENTHA PULEGIUM, MOSCHUS, BENZINUM, SEPIA, BARYTA CARBONICA, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, THYROIDINUM (SUIS), PYRIDOXINUM HYDROCHLORICUM, GELSEMIUM SEMPERVIRENS, NATRUM CARBONICUM, NUX VOMICA, STAPHYSAGRIA
Manufacturer Nucleic Products, LLC
Product type HUMAN OTC DRUG
SPL set ID b95050f2-f40d-4e84-8752-4d7ad75390c9
SPL ID 4e326cd0-c586-4d82-80ef-0ae5dd294dcc
Version 4
Effective date 2025-03-20
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:48:00 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Hypothaltem openfda.brand_name generic name EUPATORIUM PERFOLIATUM, BERBERIS VULGARIS, MENTHA PULEGIUM, MOSCHUS, BENZINUM, SEPIA, BARYTA CARBONICA, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, THYROIDINUM (SUIS), PYRIDOXINUM HYDROCHLORICUM, GELSEMIUM SEMPERVIRENS, NATRUM CARBONICUM, NUX VOMICA, STAPHYSAGRIA openfda.generic_name manufacturer name Nucleic Products, LLC openfda.manufacturer_name ndc package 75053-0010-1 openfda.package_ndc ndc product 75053-0010 openfda.product_ndc ndc11 package 75053001001 derived:openfda.package_ndc spl id 4e326cd0-c586-4d82-80ef-0ae5dd294dcc id spl set id b95050f2-f40d-4e84-8752-4d7ad75390c9 set_id unii 269XH13919 openfda.unii unii 0B4FDL9I6P openfda.unii unii 00543AP1JV openfda.unii unii 8KFK4W7KP7 openfda.unii unii 1TH8Q20J0U openfda.unii unii QDL83WN8C2 openfda.unii unii 6P669D8HQ8 openfda.unii unii 639KR60Q1Q openfda.unii unii L0PFEMQ1DT openfda.unii unii J64922108F openfda.unii unii 398IYQ16YV openfda.unii unii 1W0775VX6E openfda.unii unii 45P3261C7T openfda.unii unii 68Y4CF58BV openfda.unii unii 5Q6Y7K4846 openfda.unii unii N6R0856Z79 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: As with any drug, ask a doctor before use if pregnant or nursing. Consult a physician if Symptoms persist for more than 7 days or worsen. Keep this and all medications out of the reach of children In case of accidental overdose, contact a medical professional or a poison control center immediately. Do not use if seal is broken or missing. This product does not contain sugar, starch, preservatives, artificial flavors or additives, and no wheat, gluten , soy, or milk derivatives.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.