FDA label 69289980-07fc-49ae-8948-726954bb97b0

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
944ef64b-3970-432b-b151-e2aea0730374
SPL ID
69289980-07fc-49ae-8948-726954bb97b0
Version
2
Effective date
2022-01-24
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 02:38:52

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 According to homeopathic principles, symptoms may temporarily worsen before improving (initial exacerbation of symptoms). Do not exceed recommended dosage. Not intended for children under 2. A persistent cough may be a sign of a serious condition. Do not use in case of hypersensitivity/allergy to the ingredients If pregnant, trying to get pregnant or breast feeding, ask a health professional before use. Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if symptoms worsen or persist for more than 72 hours there is a fever of 102°F or greater

Reported adverse events (FAERS/openFDA)#

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