Allergies and Hay Fever Reliever

Manufacturer
King Bio Inc.
Effective date
2024-11-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:49:00

Label at a glance#

ProductAllergies and Hay Fever Reliever
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA WHOLE, ARSENIC TRIOXIDE, ARISAEMA TRIPHYLLUM ROOT, ARUNDO PLINIANA ROOT, EUPHRASIA STRICTA, GALPHIMIA GLAUCA FLOWERING TOP, HISTAMINE DIHYDROCHLORIDE, POTASSIUM DICHROMATE, NAPHTHALENE, SODIUM CHLORIDE, SCHOENOCAULON OFFICINALE SEED, SOLIDAGO VIRGAUREA FLOWERING TOP, LOBARIA PULMONARIA, WYETHIA HELENIOIDES ROOT
Label structure9 sections

Indications and uses

For temporary relief of allergies in general including hay fever symptoms:  nasal and sinus congestion  runny nose sneezing  coughing  watery eyes  As per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image: Allergies.jpg

Dosage and administration

Initially, depress pump until primed. Spray one dose directly into mouth. Adults: 3 sprays 3 times per day. Children ages 6-12: 2 sprays 3 times per day. Consult a physician for use in children under 6 years of age. Use additionally as needed, up to 6 times per day. Reference image: Allergies.jpg

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Initially, depress pump until
primed.

Spray one dose directly into
mouth.

Adults: 3 sprays 3 times per
day.

Children ages 6-12: 2 sprays 3
times per day.

Consult a physician for use in
children under 6 years of age.

Use additionally as needed, up
to 6 times per day.

Reference image: Allergies.jpg

OTHER SAFETY INFORMATION

Other information

Tamper resistant for your protection.

Use only if safety seal is intact.

Keep carton for complete drug facts and product information.

Questions? Call 866.298.2740

King Bio, Inc. 3 Westside Drive

Asheville, NC 2806 USA

FDA Reg. #1053442

For latest product information and instructions: www.DrKings.com

Reference image: Allergies.jpg

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citrus Extract (ascorbic acid, citric acid, citrus aurantium amara fruit extract, citrus aurantium sinensis peel extract, citrus reticulata fruit extact, demineralized water, glycerin, lactic acid), Honeysuckle (Lonicera japonica), Polylysine, Purified Water, Shagbark Hickory (Carya Ovata) Bark Extract, Steviol (Steviol Glycosides).

Reference image: Allergies.jpg

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Equal volumes of each HPUS ingredient in 10X, 30X, and 1LM
potencies.

Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Galphimia glauca,
Histaminum hydrochloricum, Kali bichromicum, Naphthalinum, Natrum muriaticum, Sabadilla, Solidago virgaurea, Sticta pulmonaria, 
Wyethia helenioides.

HPUS” indicates the active ingredients are in the official
Homeopathic Pharmacopeia of the United States.

Reference image: Allergies.jpg

Uses

INDICATIONS & USAGE SECTION

For temporary relief of allergies in general including hay
fever symptoms: 

nasal and sinus congestion 

runny nose

sneezing 

coughing 

watery eyes 

As per various homeopathic materia medicas. Claims based
on traditional homeopathic practice, not accepted medical
evidence. These uses have not been evaluated by the FDA,
and product has not been clinically tested.

Reference image: Allergies.jpg

Warnings

WARNINGS SECTION

Stop use and consult a physician if symptoms worsen or
persist for more than 7 days.

If pregnant or breast-feeding, ask a healthcare professional
before use.
Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center immediately.

Reference image: Allergies.jpg

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center immediately.

Reference image: Allergies.jpg

OTC - PURPOSE SECTION

Equal volumes of each HPUS ingredient in 10X, 30X, and 1LM
potencies.

Allium cepa............. runny nose; itchy eyes, ears, nose or throat
Ambrosia artemisiaefolia..................nasal and sinus congestion
Arsenicum album ...................................... exhaustion, hay fever
Arum triphyllum .......................swollen glands, nasal congestion
Arundo mauritanica ......................... itching and burning in nose,
ears, or roof of mouth
Euphrasia officinalis.........................sinus irritation and pressure
Galphimia glauca..........................................excessive sneezing
Histaminum hydrochloricum .............symptoms of allergic origin
Kali bichromicum ............................... nasal congestion, sinusitis
Naphthalinum ....................................................sneezing, cough
Natrum muriaticum..........................................itchy, watery eyes
Sabadilla .......................................sore throat, hay fever, vertigo
Solidago virgaurea ...................inflammation, mucus congestion
Sticta pulmonaria...................congestion, dull headache, rhinitis
Wyethia helenioides ............... postnasal drip, bronchial irritation

HPUS” indicates the active ingredients are in the official
Homeopathic Pharmacopeia of the United States.

Reference image: Allergies.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description Allergies.jpgimage description Allergies.jpg

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-280557955-2805-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
999ff14e-86b8-4f33-aece-072f4942d49fb99f71e3-a0ab-464f-9d87-c6ab171096ea2025-05-16WarningsExact identifier
spl set id: b99f71e3-a0ab-464f-9d87-c6ab171096ea

Reported adverse events (FAERS/openFDA)#

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