NUVICARE-ALLERGY RELIEF LORATADINE TABLETS, 10 MG- loratadine tablet

Nuvicare-Allergy Relief Loratadine Tablets, 10 mg by

Drug Labeling and Warnings

Nuvicare-Allergy Relief Loratadine Tablets, 10 mg by is a Otc medication manufactured, distributed, or labeled by NUVICARE LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Active Ingredient (in each tablet)

Loratadine, 10 mg 

PURPOSE

Purpose

Antihistamine

Uses

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

• runny nose
• sneezing
• itchy, watery eyes
• itching of the nose or throat

Warnings

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

ASK DOCTOR

Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.

WHEN USING

When using this product do not take more than directed. Taking more than directed may cause drowsiness.

STOP USE

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.

PREGNANCY OR BREAST FEEDING

If pregnanct or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

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 age: Ask a doctor. 
Consumers with liver or kidney disease: Ask a doctor

Other Information

• Store between 20° to 25°C (68° to 77°F) (see USP Controlled Room Temperature)
•  Protect from excessive moisture

Inactive ingredients

Lactose monohydrate, magnesium stearate, povidone, maize starch, purified water.

QUESTIONS

Questions or comments?

Call 1(718) 337-8733 or email: support@nuvicare.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NUVICARE-ALLERGY RELIEF LORATADINE TABLETS, 10 MG 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84324-027
Route of Administration	oral

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
povidone (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	P;10
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84324-027-01	100 in 1 BOTTLE; Type 0: Not a Combination Product	07/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA214684	07/01/2025

Labeler - NUVICARE LLC (119257565)