FDA label 76316dee-cf92-4387-bbfd-98c1e1e6463d

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
e8a8d1f4-9c59-4358-a854-efcc123a0e74
SPL ID
76316dee-cf92-4387-bbfd-98c1e1e6463d
Version
3
Effective date
2020-10-07
Source export date
2026-10-12
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/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:53:04

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.