Allergy Maximum Strength

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: Allergy Maximum Strength
Generic name: URTICA DIOICA, ALTHAEA OFFICINALIS ROOT, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND SILICON DIOXIDE
Manufacturer: Forces of Nature
Product type: HUMAN OTC DRUG
SPL set ID: 122ca23e-43f1-4e5c-afc2-1418b1717679
SPL ID: 4b453b93-21bd-b234-e063-6294a90afd0b
Version: 4
Effective date: 2026-02-20
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:56:48

Harmonized routes table
Harmonized routes
SUBLINGUAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Allergy Maximum Strength	openfda.brand_name
generic name		URTICA DIOICA, ALTHAEA OFFICINALIS ROOT, INULA HELENIUM ROOT, ANGELICA ARCHANGELICA ROOT, PINE NEEDLE OIL (PINUS SYLVESTRIS), SODIUM CHLORIDE, AND SILICON DIOXIDE	openfda.generic_name
manufacturer name		Forces of Nature	openfda.manufacturer_name
ndc	package	51393-5001-3	openfda.package_ndc
ndc	package	51393-5001-1	openfda.package_ndc
ndc	product	51393-5001	openfda.product_ndc
ndc11	package	51393500101	derived:openfda.package_ndc
ndc11	package	51393500103	derived:openfda.package_ndc
spl id		4b453b93-21bd-b234-e063-6294a90afd0b	id
spl set id		122ca23e-43f1-4e5c-afc2-1418b1717679	set_id
unii		E55SMD6DA8	openfda.unii
unii		710FLW4U46	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		5EXL5H740Y	openfda.unii
unii		DTN01M69SN	openfda.unii
unii		TRW2FUF47H	openfda.unii

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 oral (sublingual) use. Ask a doctor before use in children under 3 years of age. Stop use and ask doctor if symptoms persist for more than 3 days or worsen. When using this product, rinse right away with water if it gets in the eyes. If pregnant or breast-feeding ask a doctor before use. Keep out of reach of children.

Reported adverse events (FAERS/openFDA)#

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