MEDI-FIRST PLUS EXTRA STRENGTH NON-ASPIRIN- acetaminophen tablet, film coated 
MEDI-FIRST EXTRA STRENGTH NON-ASPIRIN- acetaminophen tablet, film coated 
MEDIQUE EXTRA STRENGTH APAP- acetaminophen tablet, film coated 
Unifirst First Aid Corporation

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Acetaminophen 500 mg

Drug Facts

Active Ingredient (in each tablet)

Acetaminophen 500 mg

Purpose

Pain reliever / fever reducer

Uses

temporarily relieves minor aches and pains due to:

■ headache

■ muscular aches

■ backache

■ minor pain of arthritis

■ 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 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.

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 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 information

■ store at room temperature 59º-86ºF (15º-30ºC)

■ tamper-evident sealed packets

■ do not use any opened or torn packets

Inactive ingredients

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

* May contain

Medique

Extra Strength APAP

Non-Aspirin Tablets

THIS PACKAGE IS FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN.

Pain Reliever / Fever Reducer • Acetaminophen 500 mg

Compare active ingredient to Tylenol®

Registered McNeil Products

Tamper Evident Unit Dose Packets

24 Tablets

(12 x 2)

175 APAPXS 17564 11-6-23 GR175R 90433 11-6-23 GR175R 80433 11-6-23 GR

MEDI-FIRST PLUS EXTRA STRENGTH NON-ASPIRIN 
acetaminophen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-274
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE K30 (UNII: U725QWY32X)  
Product Characteristics
Colorwhite ((White to Off-White)) Scoreno score
ShapeROUNDSize12mm
FlavorImprint Code G552
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-274-3350 in 1 BOX03/28/2024
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-274-48125 in 1 BOX03/28/2024
22 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01303/28/2024
MEDI-FIRST EXTRA STRENGTH NON-ASPIRIN 
acetaminophen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-273
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STARCH, CORN (UNII: O8232NY3SJ)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE K30 (UNII: U725QWY32X)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
Colorwhite ((White to Off-White)) Scoreno score
ShapeROUNDSize12mm
FlavorImprint Code G552
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-273-13250 in 1 BOX03/28/2024
1NDC:47682-273-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-273-3350 in 1 BOX03/28/2024
2NDC:47682-273-992 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-273-48125 in 1 BOX03/28/2024
3NDC:47682-273-992 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-273-5025 in 1 BOX03/28/2024
4NDC:47682-273-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01303/28/2024
MEDIQUE EXTRA STRENGTH APAP 
acetaminophen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-272
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
STEARIC ACID (UNII: 4ELV7Z65AP)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
STARCH, CORN (UNII: O8232NY3SJ)  
POVIDONE K30 (UNII: U725QWY32X)  
Product Characteristics
Colorwhite ((White to Off-White)) Scoreno score
ShapeROUNDSize12mm
FlavorImprint Code G552
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:47682-272-13250 in 1 BOX03/28/2024
1NDC:47682-272-992 in 1 PACKET; Type 0: Not a Combination Product
2NDC:47682-272-3350 in 1 BOX03/28/2024
2NDC:47682-272-992 in 1 PACKET; Type 0: Not a Combination Product
3NDC:47682-272-48125 in 1 BOX03/28/2024
3NDC:47682-272-992 in 1 PACKET; Type 0: Not a Combination Product
4NDC:47682-272-6412 in 1 BOX03/28/2024
4NDC:47682-272-992 in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01303/28/2024
Labeler - Unifirst First Aid Corporation (832947092)
Establishment
NameAddressID/FEIBusiness Operations
Prestige Packaging080667761pack(47682-272, 47682-273, 47682-274)
Establishment
NameAddressID/FEIBusiness Operations
Medique Products086911794pack(47682-272, 47682-273, 47682-274)

Revised: 3/2024
Document Id: 14bcbaf9-76b7-f8ba-e063-6294a90a91f6
Set id: 14bcbaf9-76b6-f8ba-e063-6294a90a91f6
Version: 1
Effective Time: 20240328
 
Unifirst First Aid Corporation