ALL DAY ALLERGY RELIEF- loratadine tablet 
Safeway, Inc.

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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 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

COMPARE TO Claritin® 24 Hour active ingredient†

All Day Allergy Relief

LORATADINE TABLETS, 10mg

Antihistamine

Non-Drowsy*

Indoor & Outdoor Allergies

24 hour relief of:

TABLETS

*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:

BETTER LIVING BRANDS LLC

P.O. BOX 99, PLEASANTON, CA 94566-0009


Package Label

Loratadine, USP 10 mg

SIGNATURE CARE All Day Allergy Relief

ALL DAY ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-914
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:21130-914-1010 in 1 CARTON03/31/2023
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:21130-914-601 in 1 BOX03/31/2023
260 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:21130-914-121 in 1 BOX03/31/2023
3120 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520903/31/2023
Labeler - Safeway, Inc. (009137209)

Revised: 5/2023
Document Id: caec4d72-3aae-469d-9682-4b5fd07f01c9
Set id: 9e581ae1-d1e6-4038-86e8-fd0c5ab9878a
Version: 4
Effective Time: 20230512
 
Safeway, Inc.