CHILDRENS LORATADINE
CHILDRENS LORATADINE is an FDA drug label for the active ingredient LORATADINE manufactured by CVS PHARMACY, INC 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 20190226.
Generic: LORATADINE
Manufacturer: CVS PHARMACY, INC
Product Type: HUMAN OTC DRUG
Route: ORAL
Dosage Form:
NDC: 69842-953
Application: ANDA210088
Effective: 20190226
Active Ingredients: Active ingredient (in each tablet) Loratadine USP, 5 mg
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 chew 2 tablets daily; not more than 2 tablets in 24 hours children 2 to under 6 years of age chew 1 tablet daily; not more than 1 tablet in 24 hours children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor
Contraindications
Not available.
Warnings
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. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Adverse Reactions
Not available.
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