Medics Choice Eye Drops Original Redness Reliever

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
Medics Choice Eye Drops Original Redness Reliever
Generic name
TETRAHYDROZOLINE HYDROCHLORIDE
Manufacturer
KC Pharmaceuticals, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
e42cb1bf-b985-4a1b-9a9b-ac27c2a5d7be
SPL ID
4748ccb8-2816-8c8c-e063-6294a90a908c
Version
4
Effective date
2025-12-30
Source export date
2026-10-30
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:41:33
Harmonized routes table
Harmonized routes
OPHTHALMIC

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 narrow angle glaucoma When using this product ■ pupils may become enlarged temporarily ■ to avoid contamination, do not touch tip of container to any surface. Replace cap after using. ■ if solution changes color or becomes cloudy, do not use ■ overuse may produce increased redness of the eye ■ remove contact lens before using Stop use and ask a doctor if you experience ■ eye pain ■ changes in vision ■ continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours If pregnant or breast-feeding , ask a health professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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