Allergy Relief by Preferred Pharmaceuticals, Inc. Drug Facts

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Preferred Pharmaceuticals, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ALLERGY RELIEF NON DROWSY- loratadine tablet 
Preferred Pharmaceuticals, 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:

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

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 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 at 20º-25ºC (68º-77ºF) (see UPS Controlled Room Temperature)
• protect from light

Inactive ingredients

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

Questions or comments?

Call 1-888-588-1418 Monday-Friday 9AM-5PM EST

Principal Display Panel

†Compare to the active ingredient in Claritin® 24 Hour

Non-drowsy*

Allergy Relief

Loratadine Tablets, USP 10 mg / Antihistamine

Indoor & outdoor  allergies

24 Hour Relief of:

• Sneezing
• Runny Nose
• Itchy, Watery Eyes
• Itchy Nose or Throat

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 CAPS IS BROKEN OR MISSING.

Distributed by:

Camber Consumer Care Inc., Piscataway, NJ 08854, USA

Repackaged By: Preferred Pharmaceuticals Inc.

Package Label

CAMBER CONSUMER CARE Non-Drowsy Allergy Relief

ALLERGY RELIEF  NON DROWSY
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68788-7769(NDC: 69230-317)
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)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)

Product Characteristics
Color	WHITE	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	439
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68788-7769-0	10 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/2020	12/25/2024
2	NDC: 68788-7769-1	14 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/2020	12/25/2025
3	NDC: 68788-7769-5	15 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/2020	12/25/2025
4	NDC: 68788-7769-3	30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/2020	12/25/2025
5	NDC: 68788-7769-9	90 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/03/2020	12/25/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA075209	08/03/2020	12/25/2025

Labeler - Preferred Pharmaceuticals, Inc. (791119022)

Registrant - Preferred Pharmaceuticals, Inc. (791119022)

Establishment
Name	Address	ID/FEI	Business Operations
Preferred Pharmaceuticals, Inc.		791119022	REPACK(68788-7769)

Revised: 1/2025

Document Id: c56a05ef-9ce9-45be-8b8c-d1d730f251aa

34390-5

Set id: 9a5ffe75-cfde-4164-b5ad-398a9e68754d

Version: 5

Effective Time: 20250110