MEDI-FIRST PLUS EXTRA STRENGTH NON ASPIRIN- acetaminophen tablet MEDIQUE EXTRA STRENGTH APAP- acetaminophen tablet MEDI-FIRST EXTRA STRENGTH NON ASPIRIN- acetaminophen tablet

Medi-First Extra Strength Non Aspirin by

Drug Labeling and Warnings

Medi-First Extra Strength Non Aspirin 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)

Acetaminophen 500 mg

PURPOSE

Purpose

Pain reliever/fever reducer

INDICATIONS & USAGE

Uses

temporarily relieves minor aches and pains due to:

• headache
• muscular aches
• minor pain of arthritis
• backache
• the common cold
• toothache
• premenstrual and menstrual cramps

temporarily reduces fever

WARNINGS

Warnings

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take:

• more than 4,000 mg in 24 hours, which is the maximum daily amount
• with other drugs containing acetaminophen
• 3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

• skin reddening
• blisters
• rash

If a skin reaction occurs, stop use and seek medical help right away.

DO NOT USE

Do not use

• with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug

contains acetaminophen, ask a doctor or pharmacist.

• if you are allergic to acetaminophen or any of the inactive ingredients in this product

ASK DOCTOR

Ask a doctor before use if

• you are taking the blood thinning drug warfarin

STOP USE

Stop use and ask a doctor if

• pain gets worse or lasts more than for more than 10 days
• fever gets worse or lasts more than 3 days
• new symptoms occur
• redness or swelling is present

These could be signs of a serious condition.

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.

Overdose Warning:

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

DOSAGE & ADMINISTRATION

Directions

• do not use more than directed (see overdose warning)

​

Adults and children: (12 years and over)

• take 2 tablets every 6 hours while symptoms last.
• do not take more than 6 tablets in 24 hours, unless directed by a doctor
• do not use for more than 10 days unless directed by a doctor

Children under 12 years: Ask a doctor

OTHER SAFETY INFORMATION

Other information

• store at room temperature 59º-86ºF (15º-30ºC)
• tamper-evident sealed packets
• do not use any opened or torn packets

INACTIVE INGREDIENT

Inactive ingredients

corn starch, hypromellose*, polyethylene glycol*, povidone, pregelatinized starch*, sodium starch glycolate*, stearic acid*, titanium dioxide*

*may contaim

QUESTIONS

Questions or comments? 1-800-634-7680

PRINCIPAL DISPLAY PANEL

Medique® Extra Strength APAP

Non-Aspirin Tablets

Tabletas sin Aspirina

Pain Reliever/Fever Reducer Acetaminophen 500 mg

Alivia el Dolor/ Reduce Ia Fiebre Acetaminofeno 500 mg

This Package is for Households without Young Children.

Este Paquete Para Hogares Sin Ninos Pequenos.

Pull to Open

Tire Para Abrir

Tamper Evident Unit Dose Packets

Empaquetado con Sellado Evidente en Dosis Unitarias

Collect MediBucks

See inside flap for more details

500 Tablets

(250 x 2)

PRINCIPAL DISPLAY PANEL

Medi-First® Extra Strength Non-Aspirin

Aches, Fever Acetaminophen 500 mg

Dolores, Fiebre Acetaminofeno 500 mg

Pain Reliever/Fever Reducer

Alivia el Dolor/ Reduce Ia Fiebre

Compare active ingredient to:

Compare el ingrediente activo con:

Extra Strength Tylenol®

Registered Trademark of McNeil Consumer Products

Marca Registrada de McNeil Consumer Products

This Package is for Households without Young Children.

Este Paquete Para Hogares Sin Ninos Pequenos.

Pull to Open

Tire Para Abrir

Tamper Evident Unit Dose Packets

Empaquetado con Sellado Evidente en Dosis Unitarias

250 Tablets

(125 x 2)

PRINCIPAL DISPLAY PANEL

Medi-First® Plus Extra Strength Non-Aspirin

Acetaminophen 500 mg

Pain Reliever/Fever Reducer

Pull to Open

This Package is for Households without Young Children.

Compare active ingredient to:

Extra StrengthTylenol®

Registered Trademark of McNeil Consumer Products

Tamper Evident

Unit Dose Packets

100 Tablets

(50 x 2)

INGREDIENTS AND APPEARANCE

MEDI-FIRST PLUS EXTRA STRENGTH NON ASPIRIN 
acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-174
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND	Size	12mm
Flavor		Imprint Code	44;148
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-174-33	50 in 1 BOX	02/01/2023
1		2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC: 47682-174-48	125 in 1 BOX	02/01/2023
2		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	02/01/2023

MEDIQUE EXTRA STRENGTH APAP 
acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-172
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND	Size	12mm
Flavor		Imprint Code	44;148
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-172-99	2 in 1 PACKET; Type 0: Not a Combination Product	02/01/2023
2	NDC: 47682-172-13	250 in 1 BOX	02/01/2023
2		2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-172-33	50 in 1 BOX	02/01/2023
3		2 in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 47682-172-48	125 in 1 BOX	02/01/2023
4		2 in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 47682-172-64	12 in 1 BOX	02/01/2023
5		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	02/01/2023

MEDI-FIRST EXTRA STRENGTH NON ASPIRIN 
acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-173
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Inactive Ingredients
Ingredient Name	Strength
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	white	Score	2 pieces
Shape	ROUND	Size	12mm
Flavor		Imprint Code	44;148
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-173-99	2 in 1 PACKET; Type 0: Not a Combination Product	02/01/2023
2	NDC: 47682-173-13	250 in 1 BOX	02/01/2023
2		2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC: 47682-173-33	50 in 1 BOX	02/01/2023
3		2 in 1 PACKET; Type 0: Not a Combination Product
4	NDC: 47682-173-48	125 in 1 BOX	02/01/2023
4		2 in 1 PACKET; Type 0: Not a Combination Product
5	NDC: 47682-173-50	25 in 1 BOX	02/01/2023
5		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	02/01/2023

Labeler - Unifirst First Aid Corporation (832947092)

Establishment
Name	Address	ID/FEI	Business Operations
Prestige Packaging		080667761	pack(47682-172, 47682-173, 47682-174)

Establishment
Name	Address	ID/FEI	Business Operations
Medique Products		086911794	pack(47682-172, 47682-173, 47682-174)