FDA label 81bf57bf-a622-496a-856f-9b37b67dcda9

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
b8787cce-8b2c-407f-974f-c0688b350728
SPL ID
81bf57bf-a622-496a-856f-9b37b67dcda9
Version
8
Effective date
2020-10-02
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 05:18:13

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.