Home FDA labels 4606546b-d6bf-ef47-e063-6294a90ad74d Natural Relief Cough and Congestion Cough and Congestion Symptom 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 Natural Relief Cough and Congestion Cough and Congestion Symptom Relief
Generic name ANTIMONIUM TARTARICUM, COCCUS CACTI, CUPRUM METALLICUM, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, KALI CARBONICUM, MEPHITIS MEPHITICA, NATRUM MURIATICUM, RUMEX CRISPUS, ZINCUM GLUCONICUM
Manufacturer TRP Company
Product type HUMAN OTC DRUG
SPL set ID 2a430f41-bd33-32af-e063-6394a90ae801
SPL ID 4606546b-d6bf-ef47-e063-6294a90ad74d
Version 2
Effective date 2025-12-15
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 06:40:49 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 · 18 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Natural Relief Cough and Congestion Cough and Congestion Symptom Relief openfda.brand_name generic name ANTIMONIUM TARTARICUM, COCCUS CACTI, CUPRUM METALLICUM, DROSERA ROTUNDIFOLIA, ECHINACEA ANGUSTIFOLIA, KALI CARBONICUM, MEPHITIS MEPHITICA, NATRUM MURIATICUM, RUMEX CRISPUS, ZINCUM GLUCONICUM openfda.generic_name manufacturer name TRP Company openfda.manufacturer_name ndc package 17312-432-23 openfda.package_ndc ndc product 17312-432 openfda.product_ndc ndc11 package 17312043223 derived:openfda.package_ndc spl id 4606546b-d6bf-ef47-e063-6294a90ad74d id spl set id 2a430f41-bd33-32af-e063-6394a90ae801 set_id unii 789U1901C5 openfda.unii unii QR44N9XPJQ openfda.unii unii LZB7TFX1LT openfda.unii unii DL6OZ476V3 openfda.unii unii 9N1RM2S62C openfda.unii unii 451W47IQ8X openfda.unii unii BQN1B9B9HA openfda.unii unii VB06AV5US8 openfda.unii unii U6WSN5SQ1Z openfda.unii unii 3BN57UN4US 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: A PHYSICIAN SHOULD ALWAYS BE CONSULTED TO RULE OUT SERIOUS CAUSES . • This product is intended to complement, not replace, standard medical treatment. • Initial worsening of symptoms may occur. • This product is intended to be taken orally. Do not use in eyes or nose.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.