LORATADINE- loratadine tablet 
Gobrands, Inc

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NON-DROWSY 24 HOUR

Allergy Relief

Loratadine Antihistamine

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 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 & children 6 years & over1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other information

● store between 20° to 25°C (68° to 77°F)

Inactive ingredients

corn starch, lactose monohydrate, magnesium stearate, povidone

Questions or comments?

1-888-333-9792

PRINCIPAL DISPLAY PANEL

label

carton

LORATADINE 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82501-1580
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONE (UNII: FZ989GH94E)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize6mm
FlavorImprint Code P10
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82501-1580-31 in 1 CARTON05/16/2022
130 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21468405/16/2022
Labeler - Gobrands, Inc (057499049)
Registrant - Spirit Pharmaceuticals LLC (179621011)

Revised: 12/2023
Document Id: 0c05574c-f99c-5d92-e063-6394a90a9d00
Set id: 1d182bd6-ad72-4352-b983-407a48c317f0
Version: 3
Effective Time: 20231208
 
Gobrands, Inc