Home FDA labels cede75c3-53de-4822-a5fc-a804c1b22a05 SINUS HP 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 SINUS HP
Generic name AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, POTASSIUM SULFATE, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID f017da22-74c2-40f4-adcc-5e84b6ea5291
SPL ID cede75c3-53de-4822-a5fc-a804c1b22a05
Version 4
Effective date 2025-12-16
Source export date 2026-09-28
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/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:56:45 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 SINUS HP openfda.brand_name generic name AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, CALCIUM SULFIDE, POTASSIUM DICHROMATE, POTASSIUM SULFATE, LYCOPODIUM CLAVATUM SPORE, MERCURIUS SOLUBILIS, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0045-1 openfda.package_ndc ndc product 43406-0045 openfda.product_ndc ndc11 package 43406004501 derived:openfda.package_ndc spl id cede75c3-53de-4822-a5fc-a804c1b22a05 id spl set id f017da22-74c2-40f4-adcc-5e84b6ea5291 set_id unii 27YLU75U4W openfda.unii unii 324Y4038G2 openfda.unii unii QDL83WN8C2 openfda.unii unii 1NT28V9397 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 451W47IQ8X openfda.unii unii 1K573LC5TV openfda.unii unii S7V92P67HO openfda.unii unii 9W34L2CQ9A openfda.unii unii T4423S18FM openfda.unii unii I76KB35JEV openfda.unii unii C88X29Y479 openfda.unii unii 1MBW07J51Q 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 WARNING: * 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 use if TAMPER EVIDENT seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.