FDA label 7f899e33-25b2-42cc-82d5-8aa58c5406f2

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
23c32084-4312-4494-8e64-f7f210126463
SPL ID
7f899e33-25b2-42cc-82d5-8aa58c5406f2
Version
2
Effective date
2015-08-07
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:41:40

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 external use only Ask a doctor before use if you have • cough that occurs with too much phlegm (mucus) • chronic cough that lasts or as occurs with smoking, asthma, or emphysema When using this product • do not heat • do not microwave • do not add to hot water or any container where heating water. May cause splattering and result in burns. • do not take by mouth or place in nostrils • do not get into eyes • do not bandage tightly • do not apply to wounds or damaged skin Stop use and ask a doctor if • cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache that lasts. These could be signs of a serious condition. • muscle aches and pains worsen, persist for more than 7 days, or clear up and occur again within a few days If pregnant or breast-feeding ask a health professional before use. Keep out of reach of children In case of accidental ingestion, 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.