Pollen Hayfever

Pollen Hayfever is an FDA-registered drug product whose active ingredient is ADRENALINUM, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM IODATUM, MUGWORT POLLEN (ARTEMISIA VULGARIS), BELLIS PERENNIS, BRASSICA SPP, CHENOPODIUM ALBUM, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, ALFALFA POLLEN (MEDICAGO SATIVA), PHLEUM PRATENSE, YELLOW DOCK POLLEN (RUMEX CRISPUS), SABADILLA, SILICEA, GOLDENROD POLLEN (SOLIDAGO CANADENSIS), DANDELION POLLEN (TARAXACUM OFFICINALE), RED CLOVER POLLEN (TRIFOLIUM PRATENSE), XANTHIUM STRUMARIUM. It is labelled by NaturalCare taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 70163-0031, label effective 20260505. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing ADRENALINUM, ALLIUM CEPA, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM IODATUM, MUGWORT POLLEN (ARTEMISIA VULGARIS), BELLIS PERENNIS, BRASSICA SPP, CHENOPODIUM ALBUM, EUPHRASIA OFFICINALIS, HISTAMINUM HYDROCHLORICUM, ALFALFA POLLEN (MEDICAGO SATIVA), PHLEUM PRATENSE, YELLOW DOCK POLLEN (RUMEX CRISPUS), SABADILLA, SILICEA, GOLDENROD POLLEN (SOLIDAGO CANADENSIS), DANDELION POLLEN (TARAXACUM OFFICINALE), RED CLOVER POLLEN (TRIFOLIUM PRATENSE), XANTHIUM STRUMARIUM are most often described in connection with: help temporarily, relieve allergy, symptoms runny, nose congestion, headache itchy, watery eyes, sneezing claims, based traditional. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

USES: May help temporarily relieve allergy symptoms ■ runny nose ■ congestion ■ headache ■ itchy, watery eyes, ■ sneezing* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

DIRECTIONS: Adults and children 12 years and over: ■ take 15 drops under the tongue every 3-4 hours. ■ sensitive persons and asthma sufferers take 1-3 drops and wait 3 hours then continue with regular dosage provided. ■ if allergy or asthma symptoms develop, discontinue use.

WARNINGS: Stop use and ask a doctor if ■ symptoms do not improve in 5 days or new symptoms appear. ■ you are an asthma sufferer with severe allergies. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is missing or open. ■ Store tightly closed at room temperature (65-80ºF)

What is Pollen Hayfever used for?
USES: May help temporarily relieve allergy symptoms ■ runny nose ■ congestion ■ headache ■ itchy, watery eyes, ■ sneezing* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Who makes Pollen Hayfever?
NaturalCare is the labeler of record for Pollen Hayfever.

What form does Pollen Hayfever come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Pollen Hayfever prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Pollen Hayfever been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.