Indications
TEMPORARILY RELIEVES THESE SYMPTOMS DUE TO HAY FEVER OR OTHR UPPER RESPIRATORY ALLERGIES: RUNNY NOSE ITCHY, WATERY EYES SNEEZING ITCHING OF THE NOSE OR THROAT
Warnings and precautions
DO NOT USE IF YOU HAVE EVER HAD AN ALLERGIC REACTION TO THIS PRODUCT OR ANY OF ITS INGREDIENTS. 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.
Pregnancy and 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 · TabletANDA076134-001 · Over the counter
- LORATADINE 1MG/ML · SyrupANDA077421-001 · Over the counter
- LORATADINE 1MG/ML · SyrupANDA075728-001 · Over the counter
At a glance
- Brand name
- Loratadine
- Route
- Oral
- Dosage form
- Capsule
- Applicant
- Marksans Pharma
- Status
- Over the counter
- FDA approval
- 23 Sept 2016
- Application
- ANDA206214-001