Allercetin

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)

Brand name
Allercetin
Generic name
EUPHRASIA OFFICINALIS, KALI IODATUM, SABADILLA, STICTA PULMONARIA, HISTAMINUM HYDROCHLORICUM, QUERCETIN, SUCCINICUM ACIDUM, AMBROSIA ARTEMISIAEFOLIA
Manufacturer
Source Naturals, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
a06106dd-4ca6-4c7f-99b3-b8e464bf59bb
SPL ID
85e768b9-7a6c-4a8f-9e15-9523963e505c
Version
4
Effective date
2024-10-31
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 02:56:22
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use for headache pain for more than 7 days. If symptoms persist, get worse, or are accompanied by a high fever, or if new symptoms occur, consult a physician, because these could be signs of a serious condition. Tamper Evident: Do not use if foil blister backing is broken. Foil backing is printed with product name and lot number. DO NOT USE IF ANY BLISTERS ARE BROKEN OR TORN. Contains milk

Reported adverse events (FAERS/openFDA)#

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