Loratadine ODT

Loratadine · Tablet, Orally Disintegrating · Oral

Over the counter

Active ingredient

Active ingredient (in each tablet) Loratadine USP 10 mg

Purpose

Purpose Antihistamine

Uses

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Warnings

Warnings

Do not use

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use

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

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctor

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

Pregnancy or breast-feeding

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 overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Directions place 1 tablet on tongue; tablet disintegrates, with or without water 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

Other information Phenylketonurics: Contains phenylalanine 2.25 mg per tablet do not use if the individual blister unit is open or torn store at 20° to 25°C (68° to 77°F) use tablet immediately after opening individual blister Complies with USP test 2 for Disintegration

Inactive ingredients

Inactive ingredients aspartame, crospovidone, mannitol, microcrystalline cellulose, peppermint, pregelatinized starch (maize), sodium stearyl fumarate

Questions?

Questions or comments? call 1-855-274-4122 Distributed by: RUGBY ® LABORATORIES Indianapolis, IN 46268 www.major-rugby.com Made in India

Label text from the FDA structured product label by Rugby Laboratories (revised Aug 7, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Loratadine ODT NDC products (13)

NDCStrength & formLabelerType
60000-950Loratadine 10 mg/1
Tablet, Orally Disintegrating
Ahold U.S.A., Inc,ANDA
46122-539Loratadine 10 mg/1
Tablet, Orally Disintegrating
Amerisource BergenANDA
58602-744Loratadine 10 mg/1
Tablet, Orally Disintegrating
Aurohealth LLCANDA
58602-821Loratadine 10 mg/1
Tablet, Orally Disintegrating
Aurohealth LLCANDA
58602-830Loratadine 10 mg/1
Tablet, Orally Disintegrating
Aurohealth LLCANDA
58602-881Loratadine 10 mg/1
Tablet, Orally Disintegrating
Aurohealth LLCANDA
21130-221Loratadine 10 mg/1
Tablet, Orally Disintegrating
Better Living Brands, LLCANDA
68016-088Loratadine 10 mg/1
Tablet, Orally Disintegrating
Chain Drug Consortium, LLCANDA
69842-085Loratadine 10 mg/1
Tablet, Orally Disintegrating
CVS Pharmacy, Inc.ANDA
53943-035Loratadine 10 mg/1
Tablet, Orally Disintegrating
DISCOUNT DRUG MARTANDA
0536-1367Loratadine 10 mg/1
Tablet, Orally Disintegrating
Rugby LaboratoriesANDA
49035-806Loratadine 10 mg/1
Tablet, Orally Disintegrating
Wal-Mart Stores, Inc.ANDA
0363-9937Loratadine 10 mg/1
Tablet, Orally Disintegrating
WALGREEN CO.ANDA

Frequently asked questions

What is Loratadine ODT used for?

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Who makes Loratadine ODT?

Loratadine ODT is listed by 10 labelers in the FDA NDC directory, including Ahold U.S.A., Inc,, Amerisource Bergen, Aurohealth LLC, Better Living Brands, LLC.