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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Mckesson Medical Surgical for the product Mckesson Loratadine (NDC 68599-4784). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - ask doctor, otc - when using, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Active ingredient (in each tablet)
Loratadine 10 mg
Purpose
Antihistamine
Uses
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies
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
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 (1-800-222-1222) right away.
Directions
Adults and children (6 years and older): 1 tablet daily; not more than 1 tablet in 24 hours.
Children under 6 years: Ask a doctor
Consumers with liver or kidney disease: Ask a doctor
Other information
Inactive ingredients
corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch.
Questions or comments?
Call 1-800-777-4908
NDC 68599-4784-6
McKesson
Loratadine 10 mg
Relieves sneezing, runny nose, itching and watering of the eyes due to upper respiratory allergies.
1 per Pack
50 Packs Per Box
MFR # 82478
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