FDA.reportPublic FDA data

Allergy

Manufacturer
Liddell Laboratories, Inc. | Apotheca Company
Effective date
2022-07-06
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
legacy-cache
Hydrated at
2026-08-01 21:57:27

Label at a glance#

ProductAllergy
Active ingredientONION, APIS MELLIFERA, ARALIA RACEMOSA ROOT, ARUNDO PLINIANA ROOT, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA, EUPHRASIA STRICTA, GELSEMIUM SEMPERVIRENS ROOT, HISTAMINE DIHYDROCHLORIDE, LYCOPODIUM CLAVATUM SPORE, TOXICODENDRON PUBESCENS LEAF, SCHOENOCAULON OFFICINALE SEED, SANGUINARIA CANADENSIS ROOT, URTICA URENS
Label structure10 sections

Indications and uses

May temporarily relieve these symptoms associated with allergies and hay fever: • runny nose • itchy, watery eyes • rash • headache • sneezing** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage and administration

Adults and children over 12:   Spray twice under the tongue three times per day.  For severe symptoms, dosage may be taken up to six times the first day. Children 12 and under:   Consult a doctor prior to use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Allium Cepa 6X, Apis Mellifica 3X, Aralia Racemosa 6X, Arundo Mauritanica 30C, Baptisia Tinctoria 3X, Echinacea (Angustifolia) 4X, Euphrasia Officinalis 6X, Gelsemium Sempervirens 200C, Histaminum Hydrochloricum 12X, Lycopodium Clavatum 6X, Rhus Tox 200C, Sabadilla 6X, Sanguinaria Canadensis 200C, Urtica Urens 3X, 200C.

USES:

OTC - PURPOSE SECTION

May temporarily relieve these symptoms associated with allergies and hay fever:

• runny nose

• itchy, watery eyes

• rash

• headache

• sneezing**


**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

If pregnant or breast feeding, ask a doctor before using product.

OTHER INFORMATION:

OTHER SAFETY INFORMATION

Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
Store at room temperature.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12:  Spray twice under the tongue three times per day.  For severe symptoms, dosage may be taken up to six times the first day.

Children 12 and under:  Consult a doctor prior to use.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve these symptoms associated with allergies and hay fever:

• runny nose

• itchy, watery eyes

• rash

• headache

• sneezing**


**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Organic alcohol 20% v/v, Purified water.

QUESTIONS:

OTC - QUESTIONS SECTION

DIST. BY

LIDDELL LABORATORIES

201 Apple Blvd.

Woodbine, IA 51579

WWW.LIDDELL.NET

1-800-460-7733

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ORAL SPRAYS

LIDDELL
LABORATORIES

EST. 1994


01 Al
Allergy


May relieve allergy + hay fever
symptoms: runny nose, itchy,
watery eyes, rash,
headache + sneezing

HOMEOPATHIC


DOCTOR FORMULATED

Readily absorbed. Safe.
No Known side effects. Easy to use.


1.0 FL OZ (30 ml)

Allergy lblAllergy lbl

Allergy ctnAllergy ctn

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50845-0205-22022-07-06C16284748780-19d75b9d0-8f05-f424-e053-dadaa90a57ceDrug Facts:
50845-0205-22022-01-28C16284748780-19d75b9d0-8f05-f424-e053-dadaa90a57ceDrug Facts:
50845-0205-22020-10-22C16284748780-19d75b9d0-8f05-f424-e053-dadaa90a57ceDrug Facts:
50845-0205-22020-01-31C16284748780-19d75b9d0-8f05-f424-e053-dadaa90a57ceDrug Facts:

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
APIS MELLIFERAACTIVE INGREDIENT7S82P3R43Z2
ARALIA RACEMOSA ROOTACTIVE INGREDIENTT90W4582DU2
ARUNDO PLINIANA ROOTACTIVE INGREDIENTZXE7LB03WC2
BAPTISIA TINCTORIA ROOTACTIVE INGREDIENT5EF0HWI5WU2
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US82
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WL2
GELSEMIUM SEMPERVIRENS ROOTACTIVE INGREDIENT639KR60Q1Q2
HISTAMINE DIHYDROCHLORIDEACTIVE INGREDIENT3POA0Q644U2
LYCOPODIUM CLAVATUM SPOREACTIVE INGREDIENTC88X29Y4792
ONIONACTIVE INGREDIENT492225Q21H2
SANGUINARIA CANADENSIS ROOTACTIVE INGREDIENTN9288CD5082
SCHOENOCAULON OFFICINALE SEEDACTIVE INGREDIENT6NAF1689IO2
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7A2
URTICA URENSACTIVE INGREDIENTIHN2NQ5OF92
APIS MELLIFERAACTIVE MOIETY7S82P3R43Z2
ARALIA RACEMOSA ROOTACTIVE MOIETYT90W4582DU2
ARUNDO PLINIANA ROOTACTIVE MOIETYZXE7LB03WC2
BAPTISIA TINCTORIA ROOTACTIVE MOIETY5EF0HWI5WU2
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US82
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WL2
GELSEMIUM SEMPERVIRENS ROOTACTIVE MOIETY639KR60Q1Q2
HISTAMINEACTIVE MOIETY820484N8I32
LYCOPODIUM CLAVATUM SPOREACTIVE MOIETYC88X29Y4792
ONIONACTIVE MOIETY492225Q21H2
SANGUINARIA CANADENSIS ROOTACTIVE MOIETYN9288CD5082
SCHOENOCAULON OFFICINALE SEEDACTIVE MOIETY6NAF1689IO2
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7A2
URTICA URENSACTIVE MOIETYIHN2NQ5OF92
ALCOHOLINACTIVE INGREDIENT3K9958V90M2
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50845-020550845-0205-1, 50845-0205-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ONION492225Q21HACTIB
APIS MELLIFERA7S82P3R43ZACTIB
ARALIA RACEMOSA ROOTT90W4582DUACTIB
ARUNDO PLINIANA ROOTZXE7LB03WCACTIB
BAPTISIA TINCTORIA ROOT5EF0HWI5WUACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
EUPHRASIA STRICTAC9642I91WLACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
HISTAMINE DIHYDROCHLORIDE3POA0Q644UACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
TOXICODENDRON PUBESCENS LEAF6IO182RP7AACTIB
SCHOENOCAULON OFFICINALE SEED6NAF1689IOACTIB
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB
URTICA URENSIHN2NQ5OF9ACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
ALCOHOLALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSYRUP / ORAL21000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MJELLY / VAGINALNAExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MTABLET, DELAYED RELEASE / ORALNAExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / ORAL6624 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / BUCCAL679 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / RECTAL898 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / ORAL681 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / SUBLINGUAL397 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAMUSCULAR1000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / RESPIRATORY (INHALATION)5 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TRANSDERMAL49.37 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAMUSCULAR1491 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MMOUTHWASH / BUCCAL200 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSHAMPOO / TOPICAL714 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAMUSCULAR400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TRANSDERMAL3675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE / ORAL882 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / RESPIRATORY (INHALATION)0.08 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVENOUS99 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVASCULAR100 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / NASAL70 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLOTION / TOPICAL25 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / ORAL210 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / INTRAVENOUS6405 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MELIXIR / ORAL13675 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / INTRAVESICAL7892 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / TRANSDERMAL90 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY, METERED / SUBLINGUAL29 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, SOLUTION / SUBCUTANEOUS6.1 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / DENTAL12.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPOWDER, FOR SOLUTION / TOPICAL40 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION, EMULSION / INTRAVENOUS520 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / ORAL150.68 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / INTRAVENOUS92 %w/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION, CONCENTRATE / INTRAVENOUS4000 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MINJECTION / SUBCUTANEOUS149 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / ORAL3563 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MPASTE / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSUSPENSION / RECTAL0.35 %v/vExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MDROPS / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / DENTAL1.8 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, METERED / RESPIRATORY (INHALATION)26664 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MAEROSOL, SPRAY / RESPIRATORY (INHALATION)35.75 %w/wExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCAPSULE, EXTENDED RELEASE / ORAL8 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MCONCENTRATE / ORAL198 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MGEL / TRANSDERMAL7360 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MLIQUID / INTRAVENOUS400 mgExact identifier — unii candidate
59 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSOLUTION / NASAL10 mg/1mlExact identifier — unii candidate
59 equally ranked IID candidates

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
40a7b0c2-2c1a-49bc-bd53-5752f7f1e610a457a96d-32ea-4667-80df-1aac5738cb282022-07-06WarningsExact identifier
spl id: 40a7b0c2-2c1a-49bc-bd53-5752f7f1e610
spl set id: a457a96d-32ea-4667-80df-1aac5738cb28

Reported adverse events (FAERS/openFDA)#

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