FDA label 4fb82880-2d17-48ad-aa2d-cdbacdff7348

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
3f0ddebd-7d36-43cb-ba40-45998546a7a7
SPL ID
4fb82880-2d17-48ad-aa2d-cdbacdff7348
Version
7
Effective date
2020-07-10
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:34:36

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). Use only if single-use dropper is intact. To avoid contamination, do not touch the tip of the dropper to any surface. Do not reuse. Once opened, discard. Contact wearers: consult a physician prior to using.

Reported adverse events (FAERS/openFDA)#

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