Guaifed

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
Guaifed
Generic name
GUAIFENESIN
Manufacturer
Aldama Pharmaceuticals, Inc
Product type
HUMAN OTC DRUG
SPL set ID
38f37272-2084-a33b-e063-6294a90ac150
SPL ID
58b32f6f-2554-884f-e063-6294a90a6bdd
Version
7
Effective date
2026-08-10
Source export date
2026-09-28
Source partition
2
Source file
https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:15:29
Harmonized routes table
Harmonized routes
ORAL

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 Do not use: if you ever had an allergic reaction to any of the ingredients in this product ​ Ask a doctor before use if you have cough that occurs with too much phlegm (mucus) cough that last or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

Reported adverse events (FAERS/openFDA)#

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