Home FDA labels c72e26cf-59a9-fae7-e053-2a95a90a6a00 UNDA 4 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 UNDA 4
Generic name LAURUS NOBILIS, CONDURANGO, RHAMNUS FRANGULA, MENYANTHES TRIFOLIATA, ABSINTHIUM, JATEORHIZA PALMATA, ARGENTUM METALLICUM, ANTIMONIUM CRUDUM
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 1777c76b-5329-3c7b-e054-00144ff88e88
SPL ID c72e26cf-59a9-fae7-e053-2a95a90a6a00
Version 7
Effective date 2021-07-15
Source export date 2026-09-28
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:27:00 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name UNDA 4 openfda.brand_name brand name UNDA 50 openfda.brand_name generic name BOLDO LEAF, SENNA LEAFLET, CARDUUS MARIANUS, MILLEFOLIUM, ALUMINIUM METALLICUM, ARGENTUM METALLICUM openfda.generic_name generic name LAURUS NOBILIS, CONDURANGO, RHAMNUS FRANGULA, MENYANTHES TRIFOLIATA, ABSINTHIUM, JATEORHIZA PALMATA, ARGENTUM METALLICUM, ANTIMONIUM CRUDUM openfda.generic_name manufacturer name Seroyal USA openfda.manufacturer_name ndc package 62106-1103-8 openfda.package_ndc ndc package 62106-1149-8 openfda.package_ndc ndc product 62106-1103 openfda.product_ndc ndc product 62106-1149 openfda.product_ndc ndc11 package 62106114908 derived:openfda.package_ndc ndc11 package 62106110308 derived:openfda.package_ndc spl id c72e26cf-59a9-fae7-e053-2a95a90a6a00 id spl set id 1777c76b-5329-3c7b-e054-00144ff88e88 set_id unii 2FXJ6SW4PK openfda.unii unii 3M4G523W1G openfda.unii unii S2D77IH61R openfda.unii unii F79059A38U openfda.unii unii F84709P2XV openfda.unii unii U946SH95EE openfda.unii unii WS0Y3M85RF openfda.unii unii Q4EWM09M3O openfda.unii unii 7H0QTZ446K openfda.unii unii CPD4NFA903 openfda.unii unii AK7JF626KX openfda.unii unii V36I2B8LD5 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 2 matching rows.
warnings Warnings Stop use and ask a doctor if symptoms persist or worsen. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
warnings Warnings Stop use and ask a doctor if symptomspersist or worsen If you are pregnant or breastfeeding, ask a healthcare practitioner before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.