FDA label c60421df-3235-4884-ac65-4ff6a64faf2b

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
10bf03cb-5aaf-4cb8-855e-eec36bfcc767
SPL ID
c60421df-3235-4884-ac65-4ff6a64faf2b
Version
4
Effective date
2020-10-07
Source export date
2026-09-28
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:24:45

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 tip of the bottle 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.