Home FDA labels e8917c54-f4c3-3427-e053-2995a90adbf2 Dr Talbots Infant 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 Infant Mucus Cold Relief
Generic name EUPATORIUM PERF 12X,HEPAR SULPHURIS CALCAREUM 12X,KALI BICHROMICUM 12X,MARRUBIUM VULGARE 12X,PHOSPHORUS 30X,PULSATILLA 12X,RUMEX CRISPUS 12X,SAMBUCUS NIGRA 12X,CALCAREA SULPHURICA 12X,FERRUM PHOSPHORICUM 12X
Manufacturer Talbots Pharmaceuticals Family Products, LLC.
Product type HUMAN OTC DRUG
SPL set ID e8917c54-f4c2-3427-e053-2995a90adbf2
SPL ID e8917c54-f4c3-3427-e053-2995a90adbf2
Version 1
Effective date 2022-09-13
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:09 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 · 19 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Dr Talbots Infant Mucus Cold Relief openfda.brand_name generic name EUPATORIUM PERF 12X,HEPAR SULPHURIS CALCAREUM 12X,KALI BICHROMICUM 12X,MARRUBIUM VULGARE 12X,PHOSPHORUS 30X,PULSATILLA 12X,RUMEX CRISPUS 12X,SAMBUCUS NIGRA 12X,CALCAREA SULPHURICA 12X,FERRUM PHOSPHORICUM 12X openfda.generic_name manufacturer name Talbots Pharmaceuticals Family Products, LLC. openfda.manufacturer_name ndc package 70797-320-01 openfda.package_ndc ndc product 70797-320 openfda.product_ndc ndc11 package 70797032001 derived:openfda.package_ndc spl id e8917c54-f4c3-3427-e053-2995a90adbf2 id spl set id e8917c54-f4c2-3427-e053-2995a90adbf2 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 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 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 condition. other symptoms persist for more than 7 days or worsen. Warnings
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.