FDA.reportPublic FDA data

Allergy and Hay Fever Reliever

Manufacturer
King Bio Inc
Effective date
2012-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:03:50

Label at a glance#

ProductAllergy and Hay Fever Reliever
Active ingredientONION, AMBROSIA ARTEMISIIFOLIA, ARSENIC TRIOXIDE, ARISAEMA TRIPHYLLUM ROOT, ARUNDO PLINIANA ROOT, EUPHRASIA STRICTA, NAPHTHALENE, SODIUM CHLORIDE, SCHOENOCAULON OFFICINALE SEED, WYETHIA HELENIOIDES ROOT
Label structure8 sections

Indications and uses

Uses for temporary relief of allergy and hay fever symptoms: nasal and sinus congestion, runny nose, sneezing, cough, sore throat, red, itchy or watery eyes, bronchial irritation, postnasal drip. Reference image allergy and hay fever.jpg

Dosage and administration

Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed. Adult Dose 3 pump sprays Children 2 - 12 years 2 pump sprays Reference image allergy and hay fever.jpg

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Official HPUS: Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Naphthalinum, Natrum muriaticum, Sabadilla and Wyethia helenioides.

Reference image allergy and hay fever.jpg

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Equal volumes of each ingredient in a Bio-Energetically Enhanced pure water base: 10X, 30X and LM1 potencies.

Reference image allergy and hay fever.jpg

Purpose

OTC - PURPOSE SECTION

Uses for temporary relief of allergy and hay fever symptoms:

  • nasal and sinus congestion
  • runny nose
  • sneezing
  • cough
  • sore throat
  • red, itchy or watery eyes
  • bronchial irritation
  • postnasal drip
Reference image allergy and hay fever.jpg

Dosage and Administration

DOSAGE & ADMINISTRATION SECTION

Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed.

Adult Dose 3 pump sprays

Children 2 - 12 years 2 pump sprays

Reference image allergy and hay fever.jpg

Warnings

WARNINGS SECTION

If symptoms persist or worsen, consult a physician. If pregnant or nursing, take only on advice of healthcare professional. Keep out of reach of children.

Other: Tamper resistant for your protection. Use only if safety seal is intact.

Reference image allergy and hay fever.jpg

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Reference image allergy and hay fever.jpg

Indications and Usage

INDICATIONS & USAGE SECTION


Uses for temporary relief of allergy and hay fever symptoms: nasal and sinus congestion, runny nose, sneezing, cough, sore throat, red, itchy or watery eyes, bronchial irritation, postnasal drip.

Reference image allergy and hay fever.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of label
Image of label

King Bio, Inc

3 Westside Dr.

Asheville, NC 28806

Questions? Call 800.543.3245

www.kingbio.com

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57955-5043-22020-01-31C16284748780-19d75b9d0-ef35-f424-e053-dadaa90a57ceAllergy and Hay Fever Reliever

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-5043-2Allergy and Hay Fever Reliever59 mL in 1 BOTTLE, SPRAYLIQUID591

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-5043ALLERGY AND HAY FEVER RELIEVER (ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, ARUM TRIPHYLLUM, ARUNDO MAURITANICA, EUPHRASIA OFFICINALIS, NAPHTHALINUM, NATRUM MURIATICUM, SABADILLA AND WYETHIA HELENIOIDES) LIQUID [KING BIO INC]1Legacy NDC, 1 package rows20120620_3b4bdad5-d74e-412e-b833-342157d04b64.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AMBROSIA ARTEMISIIFOLIAACTIVE INGREDIENT9W34L2CQ9A1
ARISAEMA TRIPHYLLUM ROOTACTIVE INGREDIENTDM64K844DM1
ARSENIC TRIOXIDEACTIVE INGREDIENTS7V92P67HO1
ARUNDO PLINIANA ROOTACTIVE INGREDIENTZXE7LB03WC1
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WL1
NAPHTHALENEACTIVE INGREDIENT2166IN72UN1
ONIONACTIVE INGREDIENT492225Q21H1
SCHOENOCAULON OFFICINALE SEEDACTIVE INGREDIENT6NAF1689IO1
SODIUM CHLORIDEACTIVE INGREDIENT451W47IQ8X1
WYETHIA HELENIOIDES ROOTACTIVE INGREDIENTJ10PD1AQ0N1
AMBROSIA ARTEMISIIFOLIAACTIVE MOIETY9W34L2CQ9A1
ARISAEMA TRIPHYLLUM ROOTACTIVE MOIETYDM64K844DM1
ARSENIC TRIOXIDEACTIVE MOIETYS7V92P67HO1
ARUNDO PLINIANA ROOTACTIVE MOIETYZXE7LB03WC1
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WL1
NAPHTHALENEACTIVE MOIETY2166IN72UN1
ONIONACTIVE MOIETY492225Q21H1
SCHOENOCAULON OFFICINALE SEEDACTIVE MOIETY6NAF1689IO1
SODIUM CATIONACTIVE MOIETYLYR4M0NH371
WYETHIA HELENIOIDES ROOTACTIVE MOIETYJ10PD1AQ0N1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-504357955-5043-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
ONION492225Q21HACTIB
AMBROSIA ARTEMISIIFOLIA9W34L2CQ9AACTIB
ARSENIC TRIOXIDES7V92P67HOACTIB
ARISAEMA TRIPHYLLUM ROOTDM64K844DMACTIB
ARUNDO PLINIANA ROOTZXE7LB03WCACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
NAPHTHALENE2166IN72UNACTIB
SODIUM CHLORIDE451W47IQ8XACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
WYETHIA HELENIOIDES ROOTJ10PD1AQ0NACTIB
WATER059QF0KO0RIACT

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
e9f34e51-9509-418a-bb3d-67f76c6e56fd3b4bdad5-d74e-412e-b833-342157d04b642012-06-19WarningsExact identifier
spl id: e9f34e51-9509-418a-bb3d-67f76c6e56fd
spl set id: 3b4bdad5-d74e-412e-b833-342157d04b64

Reported adverse events (FAERS/openFDA)#

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