FDA label a1e43089-21cc-4827-91dc-9d0b1ad2dd20

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
021ee685-794a-4524-b9cc-75b71e236a34
SPL ID
a1e43089-21cc-4827-91dc-9d0b1ad2dd20
Version
1
Effective date
2010-10-18
Source export date
2026-10-12
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:37:11

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

WARNING SECTION: Use only if cap and seal are unbroken. If symptoms persist for more then 3 days, consult your physician. As with any drug, if your pregnant or nursing a baby, seek the advise of a health professional before using this product. Store tightly closed in a cool, dark place. Made according to The Homeopathic Pharmacopoeia of the United States by: Remedy Makers, Pomona, CA 91768

Reported adverse events (FAERS/openFDA)#

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