MEDIQUE APAP- acetaminophen tablet, coated 
MEDI-FIRST NON-ASPIRIN- acetaminophen tablet, coated 
MEDI FIRST PLUS NON-ASPIRIN- acetaminophen tablet, coated 
DOVER AMINOPHEN- acetaminophen tablet, coated 
Unifirst First Aid Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Acetaminophen 325 mg

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

​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, maltodextrin*, microcrystalline cellulose*, polyethylene glycol, povidone, pregelatinized starch*, sodium starch glycolate, stearic acid, titanium dioxide*

* may contain

Questions or comments? 1-800-634-7680

Medi-First Non-Aspirin 325 mg Label

100

Tablets

(50 x 2)

Medi-First ®

Non-Aspirin

Pain Reliever/Fever Reducer

Aches, Fever • Acetaminophen 325mg

Pull to Open

Compare active ingredient to:

Tylenol®

Registered Trademark of McNeil Consumer Products

This Package is For Households Without Young Children

Tamper Evident Unit Dose Packets

MF Non

Medi-First Plus Non-Aspirin 325 mg Label

100 Tablets

(50 x 2's)

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 Products

Tamper Evident Unit Dose Packets

MFP Non

Dover Aminofen Label

Dover Aminofen

Pain Reliever-Fever Reducer

Acetaminophen 325mg

This package is for Households without Young Children.

Dover Pharmaceutical

Products of the highest quality and effectiveness

Tamper Resistant

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

Dover

Medique APAP 325 mg Label

Medique ®

APAP

Non-Aspirin Tablets

This Package is For Households Without young Children

Pain Reliever/Fever Reducer • Acetaminophen 325 mg

24 Tablets

(12 x 2)

Compare active ingredient to Tylenol®

Registered McNeil Consumer Products

Tamper Evident Unit Dose Packets

Medique

MEDIQUE APAP 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-112
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size11mm
FlavorImprint Code FR;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-112-326 in 1 BOX12/30/200808/01/2018
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-112-6412 in 1 BOX12/30/200804/03/2023
22 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-112-3675 in 1 BOX12/30/200804/03/2023
32 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-112-48125 in 1 BOX12/30/200804/03/2023
42 in 1 PACKET; Type 0: Not a Combination Product
5NDC:47682-112-13250 in 1 BOX12/30/200804/03/2023
52 in 1 PACKET; Type 0: Not a Combination Product
6NDC:47682-112-992 in 1 PACKET; Type 0: Not a Combination Product12/30/200804/03/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34312/30/200804/03/2023
MEDI-FIRST NON-ASPIRIN 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-113
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size11mm
FlavorImprint Code FR;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-113-3350 in 1 BOX12/30/200806/01/2023
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-113-48125 in 1 BOX12/30/200806/01/2023
22 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-113-13250 in 1 BOX12/30/200806/01/2023
32 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-113-92750 in 1 BOX12/30/200806/01/2023
42 in 1 PACKET; Type 0: Not a Combination Product
5NDC:47682-113-992 in 1 PACKET; Type 0: Not a Combination Product12/30/200806/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34312/30/200806/01/2023
MEDI FIRST PLUS NON-ASPIRIN 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-114
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size11mm
FlavorImprint Code FR;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-114-3350 in 1 BOX12/30/200806/01/2023
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-114-48125 in 1 BOX12/30/200806/01/2023
22 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34312/30/200806/01/2023
DOVER AMINOPHEN 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-115
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
HYPROMELLOSES (UNII: 3NXW29V3WO)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite (white) Scoreno score
ShapeROUND (ROUND) Size11mm
FlavorImprint Code FR;2
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-115-13250 in 1 BOX12/30/200807/01/2022
1NDC:47682-115-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-115-992 in 1 PACKET; Type 0: Not a Combination Product12/30/200807/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34312/30/200807/01/2022
Labeler - Unifirst First Aid Corporation (832947092)

Revised: 3/2023
Document Id: f6521344-c6aa-8d08-e053-2a95a90a6451
Set id: dda67533-7e9b-4724-a8e2-e996a5d6a6f8
Version: 17
Effective Time: 20230307
 
Unifirst First Aid Corporation