Indications
Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: ■ sneezing ■ runny nose ■ itchy, watery eyes ■ itching of the nose or throat.
Warnings and precautions
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 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. Pregnancy/Breastfeeding If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children Keep out of reach of children. In case of accidental overdose, contact a doctor or Poison Control Center (1-800-222-1222) immediately.
Pregnancy and breastfeeding
Pregnancy/Breastfeeding If pregnant or breast-feeding, ask a health professional before use.
Composition
- Active ingredients
- LORATADINE 10MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- LORATADINE 10MG · TabletANDA076301-001 · Over the counter
- LORATADINE 10MG · TabletANDA210722-001 · Over the counter
- LORATADINE 5MG · Tablet, orally disintegratingANDA212795-001 · Over the counter
- LORATADINE 1MG/ML · SuspensionNDA021734-001 · Discontinued
- LORATADINE 1MG/ML · SyrupANDA075505-001 · Discontinued
- LORATADINE 10MG · Tablet
At a glance
- Brand name
- Loratadine
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Apotex
- Status
- Over the counter
- FDA approval
- 14 Feb 2006
- Application
- ANDA076471-001