ALL DAY ALLERGY RELIEF- loratadine tablet 
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

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Drug Facts

Active ingredient (in each tablet)

Loratadine, USP 10 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

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 (1-800-222-1222) right away.

Directions

adults and children 6 years and over1 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

Inactive ingredients

lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

Call 1-888-309-9030

Principal Display Panel

Compare to the active ingredient in Claritin® 24 Hour**

all Day Allergy Relief

Loratadine 10 mg tablets

Antihistamine

Non-drowsy*

Indoor & outdoor allergies

24 hour relief of:

Tablets

Gluten-free

*when taken as directed, see drug facts panel

**This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® 24 Hour.

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION

DISTRIBUTED BY

OLD EAST MAIN CO

100 MISSION RIDGE

GOODLETTSVILLE, TM 37072

Package Label

Loratadine, USP 10 mg

DOLLAR GENERAL HEALTH All Day Allergy Relief

ALL DAY ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55910-718
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize6mm
FlavorImprint Code 439
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55910-718-301 in 1 BOX10/25/2023
130 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:55910-718-601 in 1 BOX10/25/2023
260 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520910/25/2023
Labeler - Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) (068331990)

Revised: 10/2023
Document Id: 8760e78a-a15c-4078-80a3-dd2f7aaf01df
Set id: 9ea4fde8-e091-412d-9de1-dd66a2ab73e4
Version: 3
Effective Time: 20231026
 
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)