Home FDA labels f98bd339-1709-6f48-e053-6394a90ad617 Baby Nighttime Mucus Plus 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 Baby Nighttime Mucus Plus Cold Relief
Generic name CALCIUM SULFIDE,PHOSPHORUS,SULFUR,RUMEX CRISPUS ROOT,SODIUM CHLORIDE,ARABICA COFFEE BEAN,ANEMONE PULSATILLA,SILICON DIOXIDE, GOLDENSEAL,ONION,BRYONIA ALBA ROOT,EUPHRASIA STRICTA AND MATRICARIA CHAMOMILLA
Manufacturer Hyland's Inc.
Product type HUMAN OTC DRUG
SPL set ID 736b2487-e81d-d172-e053-2a91aa0ab0cf
SPL ID f98bd339-1709-6f48-e053-6394a90ad617
Version 7
Effective date 2023-04-17
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:20 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 · 25 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Baby Nighttime Mucus Plus Cold Relief openfda.brand_name generic name CALCIUM SULFIDE,PHOSPHORUS,SULFUR,RUMEX CRISPUS ROOT,SODIUM CHLORIDE,ARABICA COFFEE BEAN,ANEMONE PULSATILLA,SILICON DIOXIDE, GOLDENSEAL,ONION,BRYONIA ALBA ROOT,EUPHRASIA STRICTA AND MATRICARIA CHAMOMILLA openfda.generic_name manufacturer name Hyland's Inc. openfda.manufacturer_name ndc package 54973-3371-3 openfda.package_ndc ndc package 54973-3371-1 openfda.package_ndc ndc package 54973-3371-2 openfda.package_ndc ndc product 54973-3371 openfda.product_ndc ndc11 package 54973337101 derived:openfda.package_ndc ndc11 package 54973337102 derived:openfda.package_ndc ndc11 package 54973337103 derived:openfda.package_ndc spl id f98bd339-1709-6f48-e053-6394a90ad617 id spl set id 736b2487-e81d-d172-e053-2a91aa0ab0cf set_id unii 27YLU75U4W openfda.unii unii C9642I91WL openfda.unii unii 3SW678MX72 openfda.unii unii 9N1RM2S62C openfda.unii unii ETJ7Z6XBU4 openfda.unii unii 451W47IQ8X openfda.unii unii 492225Q21H openfda.unii unii ZW3Z11D0JV openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii G0R4UBI2ZZ 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 Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. Ask a doctor before use if you have: ■ persistent or chronic cough such as asthma, chronic bronchitis or emphysema. A persistent cough may be a sign of a serious condition. ■ cough that is accompanied by excessive phlegm (mucus). Stop use and ask a doctor if: ■ symptoms persist for more than 72 hours or worsen. ■ inflammation, fever or infection is present or develops. ■ cough tends to recur or is accompanied by a fever, rash or persistent headache. Keep out of reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.