Home FDA labels d44bf234-8633-c121-e053-2a95a90ad3f7 Allergy Relief 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 Allergy Relief
Generic name ALLIUM CEPA, APIS MELLIFICA, ARALIA RACEMOSA, BLATTA ORIENTALIS, BOVISTA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, EUPHRASIA OFFICINALAS, GALPHIMIA GLAUCA, HEDERA HELIX, HYDRASTIS CANADENSIS, LUFFA OPERCULATA, NASTURTIUM AQUATICUM, OKOUBAKA, SABADILLA, SCROPHULARIA NODOSA, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE.
Manufacturer OHM PHARMA INC.
Product type HUMAN OTC DRUG
SPL set ID c3f64a9a-d2e7-4326-aeb0-22c3693f5832
SPL ID d44bf234-8633-c121-e053-2a95a90ad3f7
Version 4
Effective date 2021-12-29
Source export date 2026-10-27
Source partition 8
Source file https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-27/2eee27992d1f29d82f827fd5be42f1314ed39ce4c497af5d81435ac6656a0957/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run 20261027T193451Z
Imported at 2026-10-27 20:24:56 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Allergy Relief openfda.brand_name generic name ALLIUM CEPA, APIS MELLIFICA, ARALIA RACEMOSA, BLATTA ORIENTALIS, BOVISTA, CARDUUS MARIANUS, CHELIDONIUM MAJUS, EUPHRASIA OFFICINALAS, GALPHIMIA GLAUCA, HEDERA HELIX, HYDRASTIS CANADENSIS, LUFFA OPERCULATA, NASTURTIUM AQUATICUM, OKOUBAKA, SABADILLA, SCROPHULARIA NODOSA, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE. openfda.generic_name manufacturer name OHM PHARMA INC. openfda.manufacturer_name ndc package 66096-710-05 openfda.package_ndc ndc product 66096-710 openfda.product_ndc ndc11 package 66096071005 derived:openfda.package_ndc spl id d44bf234-8633-c121-e053-2a95a90ad3f7 id spl set id c3f64a9a-d2e7-4326-aeb0-22c3693f5832 set_id unii K2A74U428F openfda.unii unii C9642I91WL openfda.unii unii 7E889U5RNN openfda.unii unii 93PH5Q8M7E openfda.unii unii T90W4582DU openfda.unii unii 39981FM375 openfda.unii unii U946SH95EE openfda.unii unii 3D10KUA6BM openfda.unii unii C4MO6809HU openfda.unii unii 6NAF1689IO openfda.unii unii 492225Q21H openfda.unii unii ZW3Z11D0JV openfda.unii unii MK2074187Z openfda.unii unii YH89GMV676 openfda.unii unii 7S82P3R43Z openfda.unii unii 5405K23S50 openfda.unii unii 535787266D openfda.unii unii 7H443NUB2T 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: KEEP OUT OF THE REACH OF CHILDREN IF PREGNANT OR BREAST - FEEDING, ask a health professional before use. If symptons worsen or persist for more than a week, discontinue use and contact a doctor. Do not use if cap seal is broken. KEEP OUT OF THE REACH OF CHILDREN
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.