Label at a glance#

ProductWHP Hay Fever

Active ingredientGELSEMIUM SEMPERVIRENS ROOT, STRYCHNOS NUX-VOMICA SEED, ARSENIC TRIOXIDE, ONION

Label structure8 sections

Indications and uses

Temporarily relieves symptoms associated with hay fever.

Dosage and administration

Directions: Adults and children 12 years and older: 2 pills dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children 4 years to under 12 years: 1 pill dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children under 4 years: Consult a licensed practitioner.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

ALLIUM CEPA 6C

ARSENICUM ALB 6C

GELSEMIUM 6C

NUX VOM 6C

USES

OTC - PURPOSE SECTION

Temporarily relieves symptoms associated with hay fever.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

As with all medications, keep out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

ALLIUM CEPA Head cold

ARSENICUM ALB Vomiting

GELSEMIUM Lethargy

NUX VOM Vomiting

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist or recur, discontinue use. If pregnant or nursing, consult a licensed practitioner before using this product.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Directions: Adults and children 12 years and older: 2 pills dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children 4 years to under 12 years: 1 pill dissolved under tongue every 4 hours, or as directed by a licensed practitioner. Children under 4 years: Consult a licensed practitioner.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WHP Hay Fever labelWHP Hay Fever box

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139	Product name	3	20240506
e5a77e9c-c528-733a-173d-914a234c024b	Product name	5	20240506

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71919-807-14	WHP Hay Fever	1 in 1 BOX	PELLET	1		2
71919-807-14	WHP Hay Fever	1 in 1 BOTTLE, PLASTIC	PELLET	1		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71919-807	WHP HAY FEVER (ONION - ARSENIC TRIOXIDE - GELSEMIUM SEMPERVIRENS ROOT - STRYCHNOS NUX-VOMICA SEED) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]	2	Current NDC, 2 package rows	20250130_06d4d93a-eb79-99a3-e063-6394a90a8ed7.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

WHP Hay Fever
Onion - Arsenic Trioxide - Gelsemium Sempervirens Root - Strychnos Nux-Vomica Seed
LACTOSE
SUCROSE
GELSEMIUM SEMPERVIRENS ROOT
STRYCHNOS NUX-VOMICA SEED
ARSENIC TRIOXIDE
ARSENIC CATION (3+)
ONION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71919-807	71919-807-14

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
LACTOSE	J2B2A4N98G	IACT
SUCROSE	C151H8M554	IACT
GELSEMIUM SEMPERVIRENS ROOT	639KR60Q1Q	ACTIB
STRYCHNOS NUX-VOMICA SEED	269XH13919	ACTIB
ARSENIC TRIOXIDE	S7V92P67HO	ACTIB
ONION	492225Q21H	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
WHP Hay Fever	ONION - ARSENIC TRIOXIDE - GELSEMIUM SEMPERVIRENS ROOT - STRYCHNOS NUX-VOMICA SEED	Washington Homeopathic Products	06d4d93a-eb79-99a3-e063-6394a90a8ed7	2025-01-28	Warnings	Exact identifier ndc (package): 71919-807-14 ndc (product): 71919-807 ndc11 (package): 71919080714 spl id: 2cc8699a-6750-3cfe-e063-6394a90a19f3 spl set id: 06d4d93a-eb79-99a3-e063-6394a90a8ed7

Reported adverse events (FAERS/openFDA)#

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