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Allergy Relief by Allegiant Health

Medically reviewed on December 18, 2017

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: Allegiant Health
NDC Code: 69168-309

Drug Facts

Active ingredient

Loratadine 10 mg

Purpose

Antihistamine

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

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

Ask doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

When usingthis 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. You may report side effects to 1-888-952-0050

If pregnant or breast-feeding

ask a health professional before use

Keep Out of Reach of Children

In case of accidental overdose, contact a doctor or Poison Control Center immediately

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

Inactive Ingredients

colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose.

Package/Label Principal Display Panel
ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69168-309
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE 
CROSCARMELLOSE SODIUM 
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
CELLULOSE, MICROCRYSTALLINE 
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize6mm
FlavorImprint CodeLOR10
Contains    
Packaging
#Item CodePackage Description
1NDC:69168-309-085 TABLET in 1 BLISTER PACK
2NDC:69168-309-0910 TABLET in 1 BLISTER PACK
3NDC:69168-309-3030 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07647112/16/2014
Labeler - Allegiant Health (079501930)
Registrant - Allegiant Health (079501930)
Establishment
NameAddressID/FEIOperations
Allegiant Health079501930ANALYSIS(69168-309), LABEL(69168-309), MANUFACTURE(69168-309), PACK(69168-309), RELABEL(69168-309), REPACK(69168-309)

 
Allegiant Health

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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