Home FDA labels a4eea6e6-1a72-46a1-8219-c21468318ba9 ALLERGY NEW ENGLAND MIX 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 NEW ENGLAND MIX
Generic name BETULA PUBESCENS BARK, ARTEMISIA VULGARIS POLLEN, PLANTAGO LANCEOLATA POLLEN, ACER PSEUDOPLATANUS POLLEN, BETULA PUBESCENS BARK, EVERNIA PRUNASTRI BARK, ARMARANTHUS RETROFLEXUS POLLEN, PINUS MASSONIANA POLLEN, TABULIFORMIS POLLEN, AMBROSIA ARTEMISIFOLIA POLLEN,
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID b12b20c3-a7bf-4366-89da-a8023204048e
SPL ID a4eea6e6-1a72-46a1-8219-c21468318ba9
Version 6
Effective date 2025-11-13
Source export date 2026-10-12
Source partition 6
Source file https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:46:34 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 ALLERGY NEW ENGLAND MIX openfda.brand_name generic name BETULA PUBESCENS BARK, ARTEMISIA VULGARIS POLLEN, PLANTAGO LANCEOLATA POLLEN, ACER PSEUDOPLATANUS POLLEN, BETULA PUBESCENS BARK, EVERNIA PRUNASTRI BARK, ARMARANTHUS RETROFLEXUS POLLEN, PINUS MASSONIANA POLLEN, TABULIFORMIS POLLEN, AMBROSIA ARTEMISIFOLIA POLLEN, openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0106-1 openfda.package_ndc ndc product 43406-0106 openfda.product_ndc ndc11 package 43406010601 derived:openfda.package_ndc spl id a4eea6e6-1a72-46a1-8219-c21468318ba9 id spl set id b12b20c3-a7bf-4366-89da-a8023204048e set_id unii VU8C8SB23P openfda.unii unii PY0JA16R2G openfda.unii unii 9LYI4RTZ52 openfda.unii unii ANT994T71D openfda.unii unii 3R504894L9 openfda.unii unii N52MIQ81ZW openfda.unii unii 73B14PX5FW openfda.unii unii K20Y81ACO3 openfda.unii unii 60EUO12HBX openfda.unii unii DO87T1U2CI openfda.unii unii W8RT4P7T0H openfda.unii unii O3034Q5AHK openfda.unii unii D209654E9Q 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: Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away. Do not us if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.