FDA.reportPublic FDA data

Zicam Cold Remedy RapidMelts Original and Nighttime Convenience Pack

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
Zicam Cold Remedy RapidMelts Original and Nighttime Convenience Pack
Generic name
CHAMOMILLA, ZINCUM ACETICUM, ZINCUS GLUCONICUM
Manufacturer
Church & Dwight Co., Inc.
Product type
HUMAN OTC DRUG
SPL set ID
364ddb15-ab08-6270-e063-6394a90ab935
SPL ID
59f49fd5-d5bc-1ac5-e063-6294a90aa2da
Version
3
Effective date
2026-08-26
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:02
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings If you are allergic or sensitive to zinc, consult a doctor before using Stop use and ask a doctor if symptoms persist or are accompanied by a fever or new symptoms occur If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

warnings

Warnings If you are allergic or sensitive to zinc, consult a doctor before using Stop use and ask a doctor if symptoms persist or are accompanied by a fever or new symptoms occur If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.