Home FDA labels c71e791a-cfbb-6f52-e053-2995a90af4d4 Melange combination 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 Melange combination
Generic name CALCAREA SULPHURICA, CALCIUM PHOSPHORICUM, KALI MURIATICUM, KALIUM PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRIUM SULFURICUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, SILICEA
Manufacturer Seroyal USA
Product type HUMAN OTC DRUG
SPL set ID 0a071fbf-0075-4479-e054-00144ff8d46c
SPL ID c71e791a-cfbb-6f52-e053-2995a90af4d4
Version 9
Effective date 2021-07-14
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 05:48:01 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Melange combination openfda.brand_name generic name CALCAREA SULPHURICA, CALCIUM PHOSPHORICUM, KALI MURIATICUM, KALIUM PHOSPHORICUM, KALI SULPHURICUM, MAGNESIA PHOSPHORICA, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRIUM SULFURICUM, CALCAREA FLUORICA, FERRUM PHOSPHORICUM, SILICEA openfda.generic_name manufacturer name Seroyal USA openfda.manufacturer_name ndc package 62106-1235-2 openfda.package_ndc ndc product 62106-1235 openfda.product_ndc ndc11 package 62106123502 derived:openfda.package_ndc spl id c71e791a-cfbb-6f52-e053-2995a90af4d4 id spl set id 0a071fbf-0075-4479-e054-00144ff8d46c set_id unii E934B3V59H openfda.unii unii CI71S98N1Z openfda.unii unii O3B55K4YKI openfda.unii unii 0YPR65R21J openfda.unii unii HF539G9L3Q openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 451W47IQ8X openfda.unii unii 91GQH8I5F7 openfda.unii unii 1K573LC5TV openfda.unii unii 660YQ98I10 openfda.unii unii L11K75P92J openfda.unii unii 70WT22SF4B 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 ever had an allergic reaction to this product or any of its ingredients. 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.