Home FDA labels cda11a45-601a-dbac-e053-2a95a90a2c1b Dr. Talbots Mucus Cold 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 Dr. Talbots Mucus Cold Relief
Generic name EUPATORIUM PERF, HEPAR SULPHURIS CALCAREUM, KALI BICHROMICUM, MARRUBIUM VULGARE, PHOSPHORUS, PULSATILLA, RUMEX CRISPUS, SAMBUCUS NIGRA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM
Manufacturer Talbot's Pharmaceuticals Family Products, LLC.
Product type HUMAN OTC DRUG
SPL set ID 91c311b2-a22c-0db0-e053-2995a90af3ef
SPL ID cda11a45-601a-dbac-e053-2a95a90a2c1b
Version 3
Effective date 2021-10-05
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 05:55:56 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 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Dr. Talbots Mucus Cold Relief openfda.brand_name generic name EUPATORIUM PERF, HEPAR SULPHURIS CALCAREUM, KALI BICHROMICUM, MARRUBIUM VULGARE, PHOSPHORUS, PULSATILLA, RUMEX CRISPUS, SAMBUCUS NIGRA, CALCAREA SULPHURICA, FERRUM PHOSPHORICUM, KALI MURIATICUM openfda.generic_name manufacturer name Talbot's Pharmaceuticals Family Products, LLC. openfda.manufacturer_name ndc package 70797-313-01 openfda.package_ndc ndc package 70797-313-04 openfda.package_ndc ndc product 70797-313 openfda.product_ndc ndc11 package 70797031301 derived:openfda.package_ndc ndc11 package 70797031304 derived:openfda.package_ndc spl id cda11a45-601a-dbac-e053-2a95a90a2c1b id spl set id 91c311b2-a22c-0db0-e053-2995a90af3ef set_id unii 27YLU75U4W openfda.unii unii E934B3V59H openfda.unii unii 9N1RM2S62C openfda.unii unii 91GQH8I5F7 openfda.unii unii 660YQ98I10 openfda.unii unii 7A72MUN24Z openfda.unii unii T4423S18FM openfda.unii unii CT03BSA18U openfda.unii unii 1W0775VX6E openfda.unii unii I76KB35JEV 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 Warnings Do not use: for persistent or chronic cough for treating cough from asthma, smoking, or emphysema for treating cough with excessive mucus A persistent cough may be a sign of a serious condition Stop use and ask doctor if: cough/congestion lasts for more than 7 days. cough/congestion comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious confition. other symptoms persist for more than 7 days or worsen Ask a doctor before use if you are taking a prescription drug or have a serious medical condition. Please consult your physician immediately for a worsening condition. Warning
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.