MEDIQUE LORADAMED- loratadine tablet MEDI-FIRST PLUS ALLERY RELIEF- loratadine tablet

Medi-First Plus Allery Relief by

Drug Labeling and Warnings

Medi-First Plus Allery Relief by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation, Prestige Packaging, Medique Products. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient (in each tablet)

Loratadine 10 mg

PURPOSE

Purpose

Antihistamine

INDICATIONS & USAGE

Uses

Temporarily relieves these symptoms due to hay fever or other repiratory allergies

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

WARNINGS

Warnings

DO NOT USE

Do not use if you have ever 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 diease. 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 pregnant 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).

DOSAGE & ADMINISTRATION

Directions

Adults and children: (6 years and over)

1 tablet daily; not more than 1 tablet in 24 hours

Children under 6 years:

Ask a doctor

Consumers with liver or kidney disease:

Ask a doctor

OTHER SAFETY INFORMATION

Other information

• sore between 68º and 77ºF (20º and 25ºC)
• protect from excessive moisture
• tamper evident sealed packets
• do not use any opened or torn packets

INACTIVE INGREDIENT

Inactive ingredients

corn starch*, lactose monohydrate, magnesium stearate, pregelatinized corn starch*, pregelantinized starch*, sodium starch glycolate*

* may contain

QUESTIONS

Questions or comments? Call 1-800-634-7680

PRINCIPAL DISPLAY PANEL

Medique®

Loradamed

Antihistamine Laratadine 10 mg

Antistaminico Loratadina 10 mg

24-Hour Allergy Relief

24-horas alivio a las alergias

Pull to Open

Tire Para Abrir

packet not child-resistant.

Paquete no resistente a los ninos

*When taken as directed. See Drug Facts panel.

*Cuando se toma coma se indica. Ver la informacion del medicamento.

Collect Medibucks

See inside flap for more details

50 Tablets (50 x 1)

PRINCIPAL DISPLAY PANEL

Medi-First® Plus

24-Hour Allergy Relief

24-horas alivo a las alergias

Laratadine/ Loratadina 10 mg

Pull to Open

Tire Para Abrir

Antihistamine/Antistaminico

Packet is not child-resistant.

Paquete no resistente a los ninos.

*When taken as directed. See Drug Facts panel.

*Cuando se toma coma se indica. Ver la informacion del medicamento.

Compare active ingredient to:

Claritin®

Registered Trademark of Bayer Corp.

100 Tablets (100 x 1)

INGREDIENTS AND APPEARANCE

MEDIQUE LORADAMED 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-403
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
STARCH, CORN (UNII: O8232NY3SJ)
WATER (UNII: 059QF0KO0R)
MAGNESIUM STEARATE (UNII: 70097M6I30)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	G;10
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-403-50	50 in 1 BOX	06/01/2023
1		1 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-403-12	10 in 1 BOX	06/01/2023
2		1 in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-403-46	1 in 1 PACKET; Type 0: Not a Combination Product	06/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA210722	06/01/2023

MEDI-FIRST PLUS ALLERY RELIEF 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-912
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
STARCH, CORN (UNII: O8232NY3SJ)
WATER (UNII: 059QF0KO0R)
MAGNESIUM STEARATE (UNII: 70097M6I30)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	G;10
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-912-33	100 in 1 BOX	06/01/2023
1		1 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA210722	06/01/2023

Labeler - Unifirst First Aid Corporation (832947092)

Establishment
Name	Address	ID/FEI	Business Operations
Prestige Packaging		080667761	pack(47682-403, 47682-912)

Establishment
Name	Address	ID/FEI	Business Operations
Medique Products		086911794	pack(47682-403, 47682-912)