AMAZON BASIC CARE ALLERGY RELIEF
AMAZON BASIC CARE ALLERGY RELIEF is an FDA drug label for the active ingredient LORATADINE manufactured by Amazon.com Services 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 20260828.
- Generic name
- LORATADINE
- Manufacturer
- Amazon.com Services LLC
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 72288-452
- Application
- ANDA208314
- Label effective
- 20260828
About this product
AMAZON BASIC CARE ALLERGY RELIEF is an FDA-registered drug product whose active ingredient is LORATADINE. It is labelled by Amazon.com Services LLC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 72288-452, application ANDA208314, label effective 20260828. It is one of 143 FDA drug label records sharing the active ingredient LORATADINE. 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 LORATADINE are most often described in connection with: temporarily relieves, symptoms due, hay fever, upper respiratory, allergies runny, nose itchy, watery eyes, sneezing itching. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat
Dosage & Administration
Directions adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor
Warnings
Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
More products with the same ingredient
LORATADINEALLERGY RELIEF
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View labelHow products containing LORATADINE compare
FDA lists 143 drug label records with LORATADINE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Aurohealth LLC | 7 |
| — | — | Amazon.com Services LLC | 6 |
| — | — | L. Perrigo Company | 5 |
| — | — | CVS PHARMACY, INC | 4 |
| — | — | Dr. Reddy's Laboratories Inc. | 4 |
Frequently asked questions
What is AMAZON BASIC CARE ALLERGY RELIEF used for?
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat
Who makes AMAZON BASIC CARE ALLERGY RELIEF?
Amazon.com Services LLC is the labeler of record for AMAZON BASIC CARE ALLERGY RELIEF. 143 FDA label records share the active ingredient LORATADINE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does AMAZON BASIC CARE 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 AMAZON BASIC CARE 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.
Are there other products containing LORATADINE?
Yes. 143 FDA drug label records list LORATADINE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has AMAZON BASIC CARE 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.