FDA label 2a2a6bb0-9494-4e2c-ab05-833309111207

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
82041f9e-adfd-4baf-b57d-7f32922e5fb3
SPL ID
2a2a6bb0-9494-4e2c-ab05-833309111207
Version
5
Effective date
2017-02-27
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:23:18

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: For Bronchitis Discontinue use of this product and consult a doctor promptly if: symptoms do not improve within 7 days (for adults) or 5 days (for children), tend to recur, if new symptoms appear, or if symptoms are accompanied by rash, persistent headache, or persistent or chronic cough such as may occur with smoking or emphysema or if cough is accompanied by excessive phlegm (mucus). A persistent cough may be a sign of a serious condition.

Reported adverse events (FAERS/openFDA)#

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