FDA Label for Allergy Relief
View Indications, Usage & Precautions
Allergy Relief Product Label
The following document was submitted to the FDA by the labeler of this product A-s Medication Solutions. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient (In Each Tablet)
Loratadine, USP 10 mg
Purpose
Antihistamine
Uses
temporarily relieves these symptoms due to hay fever and other upper respiratory allergies:
- runny nose
- sneezing
- itching of the nose and throat
- itchy, watery eyes
Warnings
Do not use if you have ever had an allergic reaction to this
product or any of its ingredients.
Ask a doctor before use if you have liver or kidney disease.
Your doctor should determine if you need a different dose.
When using this product do not take more than directed.
Taking more than directed may cause drowsiness.
Stop use and ask a doctor if an allergic reaction to this
product occurs. Seek medical help right away.
If pregnant or breast-feeding, ask a health professional before use.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
| adults and children
12 years and over | 1 tablet daily; not more
than 1 tablet in 24 hours |
| children under 12
years of age | ask a doctor |
| consumers with liver
or kidney disease | ask a doctor |
Other Information
- TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken.
- store between 20° to 25°C (68° to 77°F)
- protect from light
Inactive Ingredients
lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate
Questions?
call 1-800-540-3765
How Supplied
Product: 50090-6164
NDC: 50090-6164-4 30 TABLET in a BOTTLE
NDC: 50090-6164-5 90 TABLET in a BOTTLE
NDC: 50090-6164-0 10 TABLET in a BOTTLE
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