Equaline Allergy Relief
- Dosage form
- TABLET
- Labeler
- United Natural Foods, Inc. dba UNFI
- Label updated
- 2024-12-10
- Retrieved
- 2026-09-07
- Active ingredients
- LORATADINE
Active ingredient (in each tablet)
Loratadine 10 mg
Purpose
Antihistamine
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
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)
Directions
|
adults and children 6 years and over |
1 tablet daily; not more than 1 tablet in 24 hours |
|
children under 6 years of age |
ask a doctor |
|
consumers with liver or kidney disease |
ask a doctor |
Other information
-
• do not use if printed foil under cap is broken or missing -
• store between 20° to 25°C (68° to 77°F)
Inactive ingredients
lactose monohydrate, magnesium stearate, povidone, pregelatinized starch
Questions or comments?
1-855-423-2630
Principal Display Panel
EQUALINE®
compare to Claritin® Tablets active ingredient
allergy relief
loratadine tablets, 10mg (antihistamine)
non-drowsy*
indoor & outdoor allergies
24 hour relief of:
• sneezing • runny nose
• itchy, watery eyes • itchy throat or nose
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.
30 tablets
30 days of relief
actual size
ORIGINAL PRESCRIPTION STRENGTH
[Image in the official label — see DailyMed source]
[Image in the official label — see DailyMed source]
DailyMed Set ID: 232053f0-737b-46b0-959f-9edb26d82cbf · Version 8
NDC: 41163-612