Home FDA labels 8dc04b42-e0be-4820-8690-4a26fe81c8b1 Cough and Mucus Night 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 Cough and Mucus Night
Generic name ANTIMONIUM TARTARICUM, AVENA SATIVA, BRYONIA (ALBA), CHAMOMILLA, DROSERA (ROTUNDIFOLIA), HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, PASSIFLORA INCARNATA, PULSATILLA (PRATENSIS), SAMBUCUS NIGRA, STANNUM METALLICUM, SULPHUR
Manufacturer NaturalCare
Product type HUMAN OTC DRUG
SPL set ID f27e3a7f-78a3-4003-95fc-0b32671df443
SPL ID 8dc04b42-e0be-4820-8690-4a26fe81c8b1
Version 1
Effective date 2026-02-02
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 05:55:58 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 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Cough and Mucus Night openfda.brand_name generic name ANTIMONIUM TARTARICUM, AVENA SATIVA, BRYONIA (ALBA), CHAMOMILLA, DROSERA (ROTUNDIFOLIA), HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, PASSIFLORA INCARNATA, PULSATILLA (PRATENSIS), SAMBUCUS NIGRA, STANNUM METALLICUM, SULPHUR openfda.generic_name manufacturer name NaturalCare openfda.manufacturer_name ndc package 70163-0024-1 openfda.package_ndc ndc package 70163-0024-2 openfda.package_ndc ndc product 70163-0024 openfda.product_ndc ndc11 package 70163002402 derived:openfda.package_ndc ndc11 package 70163002401 derived:openfda.package_ndc spl id 8dc04b42-e0be-4820-8690-4a26fe81c8b1 id spl set id f27e3a7f-78a3-4003-95fc-0b32671df443 set_id unii 387GMG9FH5 openfda.unii unii QR44N9XPJQ openfda.unii unii DL6OZ476V3 openfda.unii unii 8E272251DI openfda.unii unii ZW3Z11D0JV openfda.unii unii T7J046YI2B openfda.unii unii 70FD1KFU70 openfda.unii unii T4423S18FM openfda.unii unii CT03BSA18U openfda.unii unii MA9CQJ3F7F openfda.unii unii CLF5YFS11O openfda.unii unii G0R4UBI2ZZ 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 such as occurs with asthma ■ if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor. Stop use and ask a doctor if ■ cough persists for more than 1 week, tends to recur, or is accompanied by fever, rash or persistent headache. These could be signs of a serious condition Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is missing or open. ■ Store tightly closed at room temperature (65-80ºF)
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.