FDA.reportPublic FDA data

Eha

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
Eha
Generic name
LIDOCAINE HYDROCHLORIDE
Manufacturer
Asclemed USA, Inc.
Product type
HUMAN PRESCRIPTION DRUG
SPL set ID
09835640-55c3-4bfa-9ad3-15d37f06e871
SPL ID
7d77ecf6-5731-d43e-e053-2991aa0af0db
Version
2
Effective date
2018-11-01
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:11:28
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

Warning For external use only. Avoid contact with eyes Stop using this product and ask doctor if symptoms last for more than seven days, or clear up and occur again within a few days if redness, irritation, swelling, pain or other symptoms increase Keep out of reach of children. If swallowed, 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.