Home FDA labels 60e20997-4f40-4924-b320-cebb1e6128a9 PMS 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 PMS
Generic name APIS MELLIFICA, CHAMOMILLA, CIMICIFUGA RACEMOSA, CUPRUM METALLICUM, IGNATIA AMARA, KALI IODATUM, MAGNESIA PHOSPHORICA, OOPHORINUM (SUIS), PLATINUM METALLICUM, SEPIA, THUJA OCCIDENTALIS
Manufacturer Liddell Laboratories, Inc.
Product type HUMAN OTC DRUG
SPL set ID 575b4736-5bae-4f15-b55b-3e1fbbb613ff
SPL ID 60e20997-4f40-4924-b320-cebb1e6128a9
Version 9
Effective date 2024-07-01
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 06:07:37 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 PMS openfda.brand_name generic name APIS MELLIFICA, CHAMOMILLA, CIMICIFUGA RACEMOSA, CUPRUM METALLICUM, IGNATIA AMARA, KALI IODATUM, MAGNESIA PHOSPHORICA, OOPHORINUM (SUIS), PLATINUM METALLICUM, SEPIA, THUJA OCCIDENTALIS openfda.generic_name manufacturer name Liddell Laboratories, Inc. openfda.manufacturer_name ndc package 50845-0109-2 openfda.package_ndc ndc package 50845-0109-1 openfda.package_ndc ndc product 50845-0109 openfda.product_ndc ndc11 package 50845010901 derived:openfda.package_ndc ndc11 package 50845010902 derived:openfda.package_ndc spl id 60e20997-4f40-4924-b320-cebb1e6128a9 id spl set id 575b4736-5bae-4f15-b55b-3e1fbbb613ff set_id unii 789U1901C5 openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii HF539G9L3Q openfda.unii unii 1NM3M2487K openfda.unii unii S7YTV04R8O openfda.unii unii 1C4QK22F9J openfda.unii unii 7S82P3R43Z openfda.unii unii G0R4UBI2ZZ openfda.unii unii K73E24S6X9 openfda.unii unii 49DFR088MY 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: Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur. Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away. If pregnant or breast feeding, ask a doctor before using product. OTHER INFORMATION: Store at room temperature. Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.