Xerac AC

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
Xerac AC
Generic name
XERAC AC
Manufacturer
Person and Covey
Product type
HUMAN OTC DRUG
SPL set ID
59e37deb-01da-465f-b806-ff1a76255e71
SPL ID
44af1725-7f15-9be4-e063-6294a90a3fc8
Version
14
Effective date
2025-11-28
Source export date
2026-11-06
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/2026-11-06/90742968499056f8845d54427ea2950526b02c3f289aedd40679ed8e120a0e89/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:42:32
Harmonized routes table
Harmonized routes
TOPICAL

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 SECTION For external use only. Avoid contact with eyes. If contact occurs, wash eyes thoroughly with water. If irritation or sensitization occurs, discontinue use or contact a physician. Xerac AC may be harmful to cotton fibers and certain metals.

Reported adverse events (FAERS/openFDA)#

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