Home FDA labels f38e873c-cc3c-f701-e053-2a95a90af213 HKI 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 HKI
Generic name ATROPINUM SULPHURICUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, CALCAREA CARBONICA, COLOCYNTHIS, COCCUS CACTI, LAPIS ALBUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, ORYCTOLAGUS CUNICULUS KIDNEY, RUBIA TINCTORUM, SARSAPARILLA, URTICA URENS
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 26e048f5-8e87-51e6-e054-00144ff88e88
SPL ID f38e873c-cc3c-f701-e053-2a95a90af213
Version 5
Effective date 2023-01-31
Source export date 2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 02:02:11 Harmonized routes table Harmonized routes SUBLINGUAL
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 HKI openfda.brand_name generic name ATROPINUM SULPHURICUM, BENZOICUM ACIDUM, BERBERIS VULGARIS, CALCAREA CARBONICA, COLOCYNTHIS, COCCUS CACTI, LAPIS ALBUS, LITHIUM CARBONICUM, LYCOPODIUM CLAVATUM, ORYCTOLAGUS CUNICULUS KIDNEY, RUBIA TINCTORUM, SARSAPARILLA, URTICA URENS openfda.generic_name manufacturer name Seroyal USA openfda.manufacturer_name ndc package 62106-0625-0 openfda.package_ndc ndc product 62106-0625 openfda.product_ndc ndc11 package 62106062500 derived:openfda.package_ndc spl id f38e873c-cc3c-f701-e053-2a95a90af213 id spl set id 26e048f5-8e87-51e6-e054-00144ff88e88 set_id unii LZB7TFX1LT openfda.unii unii 2H1576D5WG openfda.unii unii 8SKN0B0MIM openfda.unii unii 1TH8Q20J0U openfda.unii unii IHN2NQ5OF9 openfda.unii unii 482QQ7H44Q openfda.unii unii 2E32821G6I openfda.unii unii 0SVP95L23G openfda.unii unii 2NVP93XVQ3 openfda.unii unii 03J5ZE7KA5 openfda.unii unii 2BMD2GNA4V openfda.unii unii C88X29Y479 openfda.unii unii 23H32AOH17 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 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. Contains Shellfish (oyster)
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.