BABY 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 MUCUS PLUS COLD RELIEF
Generic name: BRYONIA ALBA ROOT, EUPHRASIA STRICTA, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, RUMEX CRISPUS ROOT, AND SILICON DIOXIDE
Manufacturer: Hyland's Inc.
Product type: HUMAN OTC DRUG
SPL set ID: d934cc8a-1e43-4942-858a-05b5d068679a
SPL ID: 0384ed1c-8da1-f57c-e063-6394a90ad016
Version: 12
Effective date: 2023-08-22
Source export date: 2026-10-12
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:46:26

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 · 20 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		BABY MUCUS PLUS COLD RELIEF	openfda.brand_name
generic name		BRYONIA ALBA ROOT, EUPHRASIA STRICTA, CALCIUM SULFIDE, SODIUM CHLORIDE, PHOSPHORUS, ANEMONE PULSATILLA, RUMEX CRISPUS ROOT, AND SILICON DIOXIDE	openfda.generic_name
manufacturer name		Hyland's Inc.	openfda.manufacturer_name
ndc	package	54973-3284-2	openfda.package_ndc
ndc	package	54973-3284-3	openfda.package_ndc
ndc	package	54973-3284-1	openfda.package_ndc
ndc	product	54973-3284	openfda.product_ndc
ndc11	package	54973328402	derived:openfda.package_ndc
ndc11	package	54973328401	derived:openfda.package_ndc
ndc11	package	54973328403	derived:openfda.package_ndc
spl id		0384ed1c-8da1-f57c-e063-6394a90ad016	id
spl set id		d934cc8a-1e43-4942-858a-05b5d068679a	set_id
unii		27YLU75U4W	openfda.unii
unii		C9642I91WL	openfda.unii
unii		9N1RM2S62C	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		T7J046YI2B	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 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.