FDA label 1cdae0f0-ea0e-9f72-e063-6394a90a7609

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)

SPL set ID
1cdae0f0-ea0d-9f72-e063-6394a90a7609
SPL ID
1cdae0f0-ea0e-9f72-e063-6394a90a7609
Version
1
Effective date
2024-01-06
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:45:55

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

Do not give this product for persistent or chronic cough such as occurs with asthma or if cough is accompanied by excesive phlegm (mucus) unles directed by a doctor. Stop use and ask a doctor if cough persist for more than 1 week, tends to recur or is accompanied by fever, rash or persistent headache, as a persistent cough may be a sing of a serious condition. If pregnant or breast feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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