Allergy Relief Homeopathic Pollinosan

Manufacturer
Bioforce AG
Effective date
2019-08-02
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:17:34

Label at a glance#

ProductAllergy Relief Homeopathic Pollinosan
Active ingredientVISNAGA DAUCOIDES FRUIT, ARALIA RACEMOSA ROOT, GALPHIMIA GLAUCA FLOWERING TOP, LUFFA OPERCULATA FRUIT, OKOUBAKA AUBREVILLEI BARK, LARREA TRIDENTATA LEAF
Label structure11 sections

Label contents#

Full prescribing information#

Suggested Use:

OTC - PURPOSE SECTION

For the temporary relief of allergy symptoms.

Adults:

DOSAGE & ADMINISTRATION SECTION

Place 2 tablets under the tongue 3 times daily, 15 minutes before eating. Allow to slowly dissolve in the mouth. If tablets are slow to dissolve, chew and continue to absorb sublingually.

Children 6-12: Half the adult dose.

Children under 6: use Allergy Relief drops.

Note:

SPL UNCLASSIFIED SECTION

The full effect can only be felt after several days. deally beign taking shortly before the allergy season begins and continue taking throughout the period. In acute cases, take hourly, gradually reducing frequency as improvement occurs, or as directed by a physician.

Warnings:

WARNINGS SECTION

If symptoms persist for more than 7-10 days or recur, consult a physician. If pregnant or nursing a baby, seek professional advice before using this product.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

INDICATIONS & USAGE SECTION

  • Relieves hay fever
  • Relieves sneezing
  • Relieves sniffling
  • Relieves watery eyes, swollen lids
  • Relieves itchy nose, itchy skin
  • Relieves nasal congestion

Exclusive A.Vogel Formula

SPL UNCLASSIFIED SECTION

Manufactured according to Swiss Pharmaceutical Good Manufacturing Practices.

Standardized

SPL UNCLASSIFIED SECTION

Production according to Pharmaceutical GMPs

Active Ingredients :

OTC - ACTIVE INGREDIENT SECTION

      Contains equal parts of Ammi visnaga 1X (C *), Aralia racemosa 2X (N *), Cardiospermum Halicacabum 2X (N *),  Galphimia glauca 3X (C *), Luffa operculata 6X (C *), Okoubaka aubrevillei 2X (C *), Paloondo 2X (C *). Approx. 250mg lactose (milk) per tablet. ( *HPUS Class of Preparation.)

Relives hayfever symptoms without drowsiness.

SPL UNCLASSIFIED SECTION

The product's claims are based only on theories of ho,eopathy from the 1700s that are not accepted by most modern medical experts. There is no scientific evidence that the product works.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

53758-420-053758-420-0

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130364031104909GTIN-13: 0364031104909
EAN-13: 0364031104909
GTIN-12: 364031104909
UPC-A: 364031104909
GTIN storage (14 digits): 00364031104909
53758-420-0.jpg

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53758-42053758-420-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
8f233e2f-6b86-dcc3-e053-2a95a90afcd3e8d3519e-dff8-44b3-a046-a8b9136142d82019-08-02WarningsExact identifier
spl id: 8f233e2f-6b86-dcc3-e053-2a95a90afcd3
spl set id: e8d3519e-dff8-44b3-a046-a8b9136142d8

Reported adverse events (FAERS/openFDA)#

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