Dr Talbots Infant Daily Allergy Relief
Dr Talbots Infant Daily Allergy Relief is an FDA drug label for the active ingredient ALLIUM CEPA 12X,ARALIA RACEMOSA 12X,EUPHRASIA OFFICINALIS 12X,GALPHIMIA GLAUCA 12X,HISTAMINUM HYDROCHLORICUM 12X,LUFFA OPERCULATA 12X,PULSATILLA 12X,SOLIDAGO 12X,NATRUM MURIATICUM 6X manufactured by Talbot's Pharmaceuticals Family Products,LLC. administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20220912.
- Generic name
- ALLIUM CEPA 12X,ARALIA RACEMOSA 12X,EUPHRASIA OFFICINALIS 12X,GALPHIMIA GLAUCA 12X,HISTAMINUM HYDROCHLORICUM 12X,LUFFA OPERCULATA 12X,PULSATILLA 12X,SOLIDAGO 12X,NATRUM MURIATICUM 6X
- Manufacturer
- Talbot's Pharmaceuticals Family Products,LLC.
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 70797-322
- Application
- N/A
- Label effective
- 20220912
About this product
Dr Talbots Infant Daily Allergy Relief is an FDA-registered drug product whose active ingredient is ALLIUM CEPA 12X,ARALIA RACEMOSA 12X,EUPHRASIA OFFICINALIS 12X,GALPHIMIA GLAUCA 12X,HISTAMINUM HYDROCHLORICUM 12X,LUFFA OPERCULATA 12X,PULSATILLA 12X,SOLIDAGO 12X,NATRUM MURIATICUM 6X. It is labelled by Talbot's Pharmaceuticals Family Products,LLC. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 70797-322, label effective 20220912. 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.
What it is used for
Across FDA labelling, products containing ALLIUM CEPA 12X,ARALIA RACEMOSA 12X,EUPHRASIA OFFICINALIS 12X,GALPHIMIA GLAUCA 12X,HISTAMINUM HYDROCHLORICUM 12X,LUFFA OPERCULATA 12X,PULSATILLA 12X,SOLIDAGO 12X,NATRUM MURIATICUM 6X are most often described in connection with: temporrarily relieves, symptoms asscociated, hay fever, upper respiratory, itchy nose, throat watery, eyes runny, sneezing sinus. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Temporrarily relieves the symptoms asscociated with hay fever or other upper respiratory allergies, such as itchy nose and throat watery eyes runny nose sneezing sinus pain mild wheezing Uses
Dosage & Administration
DIRECTIONS For sudden onset of symptoms: Use every 15 minutes for up to 8 doses until symptoms relieved, then every 2 hours thereafter. Children 6 - 18 lbs or 3 - 8 kgs 1.25 mL every 2 hours, reduce frequency when symptoms improve Children 19 - 29 lbs or 9 - 13 kg 2.5 mL every 2 hours, reduce frequency when symptoms improve Children 30 - 90 lbs or 14 - 41 kgs 5 mL every 2 hours, reduce frequency when symptoms improve DOSAGE
Warnings
Warnings Warnings: Do not use: to treat food allergies for persistent or chronic cough for treating cough from asthma, smoking, or emphysema for treating cough with excessive mucus A persistent cough may be a sign of a serious condition. Warnings
Frequently asked questions
What is Dr Talbots Infant Daily Allergy Relief used for?
Uses Temporrarily relieves the symptoms asscociated with hay fever or other upper respiratory allergies, such as itchy nose and throat watery eyes runny nose sneezing sinus pain mild wheezing Uses
Who makes Dr Talbots Infant Daily Allergy Relief?
Talbot's Pharmaceuticals Family Products,LLC. is the labeler of record for Dr Talbots Infant Daily Allergy Relief.
What form does Dr Talbots Infant Daily Allergy Relief 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 Dr Talbots Infant Daily Allergy Relief 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 Dr Talbots Infant Daily Allergy Relief 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.