Drug Facts

Active ingredient (in each tablet)

Acetaminophen 325 mg

Purpose

Pain reliever/fever reducer

Uses

temporarily relieves minor aches and pains due to:

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

temporarily reduces fever

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

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 a doctor before use if you have

liver disease

Ask a doctor or pharmacist before use if

you are taking the blood thinning drug warfarin

Stop using and ask a doctor if

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

These could be signs of a serious condition

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

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.

Directions

do not use more than directed (see overdose warning)

Adults and children: (12 years and over)

take 2 tablets every 4 to 6 hours while symptoms last.
do not take more than 10 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 information

store at room temperature 59°-86°F (15°-30°C)
tamper-evident sealed packets
do not use any opened or torn packets

Inactive ingredients

corn starch*, hypromellose, polyethylene glycol, povidone (K-30)*, pregelatinized starch, sodium starch glycolate, stearic acid, titanium dioxide*

May contain*

Questions or comments? 1-800-634-7680

Medique Apap

Medique ®

APAP

Non-Aspirin Tablets

Tabletas sin aspirina

Pain Reliever/Fever Reducer • Acetaminophen 325 mg

Alivia el Dolor/Reduce la Fiebre • Acetaminofeno 325 mg

This Package is For Households Without young Children

Este Paquete es Para Hogares sin Ninos Pequenos

Pull to Open

Tira Para Abrir

500 Tablets

(250 x 2)

Tamper Evident Unit Dose Packets

Empaquetado con Sellado Evidente en Dosis Unitarias

145R APAP 14513 11-6-23 GR

145R APAP 14513 11-6-23 AH

Medi-First Non Aspirin

Medi-First ®

Non-Aspirin

Pain Reliever/Fever Reducer

Aches, Fever ● Acetaminophen 325 mg

Compare active ingredient to:

Tylenol®

This Package is For Households Without Young Children

Tamper Evident Unit Dose Packets

100 Tablets

(50 x 2)

145R 80333 Rev 11-6-23 GR

145R 80333 Rev 11-6-23 AH

Medi-First Plus Non Aspirin

Medi First ® Plus

Non-Aspirin

Acetaminophen 325mg

Pull to Open

This Package is For Households Without Young Children

Pain Reliever/Fever Reducer

Compare active ingredient to:

Tylenol®

Registered Trademark of McNeil Consumer

Tamper Evident Unit Dose Packets

100 Tablets

(50 x 2's)

145R 90333 Rev 11-6-22 GR

145R 90333 Rev 11-6-23 AH

Dover Aminofen

Acetaminophen 325 MG

Pain Reliever-Fever Reducer

This Package is for Households withoutn Young Children.

Dover Pharmaceutical

Products of the highest quality and effectiveness

Tamper Evident

Sealed Packets

Unit Dose Packs

500 Tablets

(250 Packets of 2)

All Dover Pharmaceutical formulas conform to federal regulations

Antihistamine free

No danger of drowsiness

Sugar Free

for safer use by diabetics

Salt free

Minimizes high blood pressure

Caffeine Free

Avoides over stimulation

145R Aminofen 1625303 11-6-23 GR

145R Aminofen 1625303 11-6-23 AH

MEDI-FIRST NON-ASPIRIN
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-058
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STEARIC ACID (UNII: 4ELV7Z65AP)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE K30 (UNII: U725QWY32X)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	white ((White to Off-White))	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	G323
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-058-13	250 in 1 BOX	03/27/2024
1	NDC:47682-058-99	2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-058-33	50 in 1 BOX	03/27/2024
2	NDC:47682-058-99	2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-058-48	125 in 1 BOX	03/27/2024
3	NDC:47682-058-99	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	03/27/2024

MEDIQUE APAP
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-057
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
POVIDONE K30 (UNII: U725QWY32X)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
STEARIC ACID (UNII: 4ELV7Z65AP)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)

Product Characteristics
Color	white ((white to Off-White))	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	G323
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-057-13	250 in 1 BOX	03/27/2024
1	NDC:47682-057-99	2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-057-36	75 in 1 BOX	03/27/2024
2	NDC:47682-057-99	2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-057-48	125 in 1 BOX	03/27/2024
3	NDC:47682-057-99	2 in 1 PACKET; Type 0: Not a Combination Product
4	NDC:47682-057-64	12 in 1 BOX	03/27/2024
4	NDC:47682-057-99	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	03/27/2024

MEDI-FIRST PLUS NON-ASPIRIN
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-059
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
POVIDONE K30 (UNII: U725QWY32X)
STEARIC ACID (UNII: 4ELV7Z65AP)
STARCH, CORN (UNII: O8232NY3SJ)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)

Product Characteristics
Color	white ((White to Off-White))	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	G323
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-059-33	50 in 1 BOX	03/27/2024
1		2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-059-48	125 in 1 BOX	03/27/2024
2		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	03/27/2024

MEDIQUE APAP
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-145
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
HYPROMELLOSES (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	AZ;234
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47682-145-32	6 in 1 BOX	12/30/2008	08/01/2018
1	NDC:47682-145-99	2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-145-64	12 in 1 BOX	12/30/2008
2	NDC:47682-145-99	2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-145-36	75 in 1 BOX	12/30/2008
3	NDC:47682-145-99	2 in 1 PACKET; Type 0: Not a Combination Product
4	NDC:47682-145-48	125 in 1 BOX	12/30/2008
4	NDC:47682-145-99	2 in 1 PACKET; Type 0: Not a Combination Product
5	NDC:47682-145-13	250 in 1 BOX	12/30/2008
5	NDC:47682-145-99	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	12/30/2008

MEDI-FIRST NON-ASPIRIN
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-803
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
HYPROMELLOSES (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	AZ;234
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:47682-803-33	50 in 1 BOX	12/30/2008
1	NDC:47682-803-99	2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-803-48	125 in 1 BOX	12/30/2008
2	NDC:47682-803-99	2 in 1 PACKET; Type 0: Not a Combination Product
3	NDC:47682-803-13	250 in 1 BOX	12/30/2008
3	NDC:47682-803-99	2 in 1 PACKET; Type 0: Not a Combination Product
4	NDC:47682-803-92	750 in 1 BOX	12/30/2008	12/01/2022
4	NDC:47682-803-99	2 in 1 PACKET; Type 0: Not a Combination Product
5	NDC:47682-803-50	25 in 1 BOX	06/03/2019
5	NDC:47682-803-99	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	12/30/2008

MEDI FIRST PLUS NON-ASPIRIN
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-903
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
HYPROMELLOSES (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	AZ;234
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-903-33	50 in 1 BOX	12/30/2008
1		2 in 1 PACKET; Type 0: Not a Combination Product
2	NDC:47682-903-48	125 in 1 BOX	12/30/2008
2		2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	12/30/2008

DOVER AMINOPHEN
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-303
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)
HYPROMELLOSES (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (ROUND)	Size	10mm
Flavor		Imprint Code	AZ;234
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-303-13	250 in 1 BOX	12/30/2008
1	NDC:47682-303-99	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	12/30/2008

DOVER AMINOFEN
acetaminophen tablet, coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:47682-060
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg

Ingredient Name	Strength
Inactive Ingredients
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
STARCH, CORN (UNII: O8232NY3SJ)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POVIDONE K30 (UNII: U725QWY32X)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white ((White to Off-White))	Score	no score
Shape	ROUND	Size	9mm
Flavor		Imprint Code	G323
Contains

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:47682-060-13	250 in 1 BOX	03/27/2024
1	NDC:47682-060-99	2 in 1 PACKET; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	03/27/2024

Labeler - Unifirst First Aid Corporation (832947092)