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.
Pollen Distress
- Manufacturer
- Liddell Laboratories, Inc. | Apotheca Company
- Effective date
- 2026-01-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:36:53
Label at a glance#
ProductPollen Distress
Active ingredientONION, APIS MELLIFERA, ARALIA RACEMOSA ROOT, ARUNDO PLINIANA ROOT, BAPTISIA TINCTORIA ROOT, ECHINACEA ANGUSTIFOLIA WHOLE, EUPHRASIA STRICTA, GELSEMIUM SEMPERVIRENS ROOT, HISTAMINE DIHYDROCHLORIDE, LYCOPODIUM CLAVATUM SPORE, TOXICODENDRON PUBESCENS LEAF, SCHOENOCAULON OFFICINALE SEED, SANGUINARIA CANADENSIS ROOT, URTICA URENS WHOLE
Label structure9 sections
Contacts and useful links#
Websitewww.liddell.net
WWW.LIDDELL.NET
WWW.LIDDELL.NETLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
(in each spray) 6.67% of Allium Cepa 6X, Apis Mellifica 6X, Aralia Racemosa 6X, Arundo Mauritanica 30C, Baptisia Tinctoria 3X, Echinacea 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.
PURPOSE
May temporarily relieve these symptoms associated with seasonal pollen distress:
• runny nose
• itchy, watery eyes
• rash
• headache
• sneezing**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
WARNINGS:
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 for more than 7 days, 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 health professional before use.
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:
In case of overdose, get medical help or call a Poison Control Center right away.
DIRECTIONS:
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:
May temporarily relieve these symptoms associated with seasonal pollen distress:
• runny nose
• itchy, watery eyes
• rash
• headache
• sneezing**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INACTIVE INGREDIENTS:
Organic alcohol 20% v/v, Purified water.
QUESTIONS:
PACKAGE LABEL DISPLAY:
ORAL SPRAYS
LIDDELL
LABORATORIES
EST. 1994
01 Pln
Pollen Distress
HOMEOPATHIC
DOCTOR FORMULATED
Readily absorbed. Safe.
No Known side effects. Easy to use.
1.0 FL OZ (30 ml)
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0363113112962 | GTIN-13: 0363113112962 EAN-13: 0363113112962 GTIN-12: 363113112962 UPC-A: 363113112962 GTIN storage (14 digits): 00363113112962 | LIDL0043 Pollen Distress CTNCPY 2-26-25.jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 3c386306-c48a-413e-bb69-70cb268496f3 | Product name | 1 | 20210727 |
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0284-1 | Pollen Distress | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 1 | |
| 50845-0284-2 | Pollen Distress | 1 in 1 CARTON | SPRAY | 1 | 1 |
Products#
Every source-derived product name is available through these pages.
- Pollen Distress
- Allium Cepa, Apis Mellifica, Aralia Racemosa, Arundo Mauritanica, Baptisia Tinctoria, Echinacea (Angustifolia), Euphrasia Officinalis, Gelsemium Sempervirens, Histaminum Hydrochloricum, Lycopodium Clavatum, Rhus Tox, Sabadilla, Sanguinaria Canadensis, Urtica Urens
- ONION
- APIS MELLIFERA
- ARALIA RACEMOSA ROOT
- ARUNDO PLINIANA ROOT
- BAPTISIA TINCTORIA ROOT
- ECHINACEA ANGUSTIFOLIA WHOLE
- ECHINACEA ANGUSTIFOLIA
- EUPHRASIA STRICTA
- GELSEMIUM SEMPERVIRENS ROOT
- HISTAMINE DIHYDROCHLORIDE
- HISTAMINE
- LYCOPODIUM CLAVATUM SPORE
- TOXICODENDRON PUBESCENS LEAF
- SCHOENOCAULON OFFICINALE SEED
- SANGUINARIA CANADENSIS ROOT
- URTICA URENS WHOLE
- URTICA URENS
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50845-0284 | 50845-0284-1, 50845-0284-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Pollen Distress | ALLIUM CEPA, APIS MELLIFICA, ARALIA RACEMOSA, ARUNDO MAURITANICA, BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), EUPHRASIA OFFICINALIS, GELSEMIUM SEMPERVIRENS, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, RHUS TOX, SABADILLA, SANGUINARIA CANADENSIS, URTICA URENS | Liddell Laboratories, Inc. | 034fcd90-81f7-4597-b58b-e2ed7047f6bd | 2026-01-26 | Warnings | 50845-0284-1 50845-0284-2 50845-0284 50845028401 50845028402 930a8c2f-6dcc-4179-8cc1-0724922b5d01 034fcd90-81f7-4597-b58b-e2ed7047f6bd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.