FDA label 7cd9dd25-6a07-3acf-e053-2991aa0ae1ca

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
3388f2c9-089f-341f-e054-00144ff8d46c
SPL ID
7cd9dd25-6a07-3acf-e053-2991aa0ae1ca
Version
2
Effective date
2018-12-12
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:21:35

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 ophtalmic use only. Keep out of the reach of chlidren. Do not use is solution changes color or becomes cloudy. Discard 30 days after opening. Stop use and ask a doctor if you experience eye pain, changes in vision, redness or irritation of the eye. If conditions persist or worsen for more than 72 hours, discontinue use and consult your physician. Do not use is cap safety band is torn or missing. Active Ingredients Chamomilla 3X HPUS

Reported adverse events (FAERS/openFDA)#

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