CURIST ALLERGY RELIEF- loratadine 10 mg tablet 
Little Pharma, Inc.

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Drug Facts

Active ingredient (in each tablet)

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

Directions

adults and children 6 years
and over
1 tablet daily; not more
than 1 tablet in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney
disease
ask a doctor

Other information

Inactive ingredients

Lactose monohydrate, magnesium stearate, sodium starch glycolate, starch maize pregelatinized

Questions or comments?

Call 1-844-243-1241 or email hi@curistrelief.com

curistrelief.com

*When taken as directed. See Drug Facts Panel.
TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken.

(CONTINUED ON BACK OF LABEL)

Distributed by: Little Pharma, Inc., New York, NY 10023
Made in India | NDC: 72559-033-48
Compare to active ingredient in Claritin®**

PEEL HERE

**This product is not manufacutred or distributed by the owner/distributor of Claritin®

REV: 033-48-01

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curist

Allergy Relief

Loratadine Tablets USP, 10 mg

Antihistamine

Indoor and Outdoor Allergies
24 Hour Relief of Runny Nose;
Sneezing; Itchy, Watery Eyes;
Itchy Nose or Throat
Non-Drowsy*

365 Tablets

loratadine artwork

CURIST ALLERGY RELIEF 
loratadine 10 mg tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72559-033
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
STARCH, CORN (UNII: O8232NY3SJ)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize6mm
FlavorImprint Code G;10
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72559-033-48365 in 1 BOTTLE; Type 0: Not a Combination Product12/12/2023
2NDC:72559-033-4790 in 1 BOTTLE; Type 0: Not a Combination Product12/12/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21072212/12/2023
Labeler - Little Pharma, Inc. (074328189)

Revised: 12/2023
Document Id: 0c53cf0f-7683-a422-e063-6394a90ab764
Set id: 0c53cf0f-7682-a422-e063-6394a90ab764
Version: 1
Effective Time: 20231212
 
Little Pharma, Inc.