FDA label b2baf22b-43da-4c6a-a1c2-a147e0730cfd

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
01b8052d-3ce1-4e71-b4f4-1b701825cd60
SPL ID
b2baf22b-43da-4c6a-a1c2-a147e0730cfd
Version
3
Effective date
2020-10-07
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:33:16

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. According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms). Replace cap tightly after every use. To avoid contamination, do not touch the plastic tip to any surface. To avoid contamination use within 30 days of opening. Expiration date only refers to unopened bottle. Contact wearers: consult a physician prior to using. If pregnant, trying to get 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 right away. Do not use: if the solution changes color or becomes cloudy Stop use and ask a doctor if: symptoms worsen or persist for more than 72 hours you experience eye pain or changes in vision

Reported adverse events (FAERS/openFDA)#

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