Home FDA labels 4e586360-b3c5-1ce0-e063-6394a90ab6b8 H-Allergy Formula 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 H-Allergy Formula
Generic name ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARUM TRIPHYLLUM, ARUNDO MAURITANICA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, KALI BICHROMICUM, NATRUM MURIATICUM, SOLIDAGO VIRGAUREA, STICTA PULMONARIA, SULPHUR, TRIFOLIUM PRATENSE, WYETHIA HELENIOIDES
Manufacturer Healing Natural Oils LLC
Product type HUMAN OTC DRUG
SPL set ID 4e586360-b3c4-1ce0-e063-6394a90ab6b8
SPL ID 4e586360-b3c5-1ce0-e063-6394a90ab6b8
Version 1
Effective date 2026-03-31
Source export date 2026-09-28
Source partition 14
Source file https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:40:50 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name H-Allergy Formula openfda.brand_name generic name ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARUM TRIPHYLLUM, ARUNDO MAURITANICA, EUPHRASIA OFFICINALIS, GALPHIMIA GLAUCA, HISTAMINUM HYDROCHLORICUM, KALI BICHROMICUM, NATRUM MURIATICUM, SOLIDAGO VIRGAUREA, STICTA PULMONARIA, SULPHUR, TRIFOLIUM PRATENSE, WYETHIA HELENIOIDES openfda.generic_name manufacturer name Healing Natural Oils LLC openfda.manufacturer_name ndc package 61077-501-59 openfda.package_ndc ndc product 61077-501 openfda.product_ndc ndc11 package 61077050159 derived:openfda.package_ndc spl id 4e586360-b3c5-1ce0-e063-6394a90ab6b8 id spl set id 4e586360-b3c4-1ce0-e063-6394a90ab6b8 set_id unii C9642I91WL openfda.unii unii 3POA0Q644U openfda.unii unii 93PH5Q8M7E openfda.unii unii 451W47IQ8X openfda.unii unii J10PD1AQ0N openfda.unii unii 9W34L2CQ9A openfda.unii unii 492225Q21H openfda.unii unii 70FD1KFU70 openfda.unii unii T4423S18FM openfda.unii unii 5405K23S50 openfda.unii unii ZXE7LB03WC openfda.unii unii 4JS0838828 openfda.unii unii D1YM0P5Z2T openfda.unii unii DM64K844DM 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 consult a physician if symptoms worsen or persist for more than 7 days If pregnant or breast-feeding , ask a healthcare professional before use Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.