ARAMARK EXTRA STRENGTH ACETAMINOPHEN- acetaminophen tablet 
Western First Aid Safety DBA Aramark

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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Aramark Extra Strength Acetaminophen

Drug Facts

Active Ingredient (in each tablet)
Acetaminophen 500 mg

Purpose
Acetaminophen ...................Pain Reliever/Fever Reducer

Uses:
Temporarily Relieves minor aches and pains
due to:
• Headache, toothaches, menstrual cramps,
  the common cold,
• muscular aches, minor pain of arthritis
  Temporarily reduces fever

Warnings:
Allergy Alert: Acetaminophen may cause a severe skin
reactions.
Symptoms may include:
• Skin reddening •Blisters •Rash
• If a skin reaction occurs, stop use and seek medical
  right away.

Liver Warning: This product contains an
acetaminophen. Severe liver damage may occur if you
take:
• more than 8 tablets in 24 hours, which is the
maximum daily amount
• 3 or more alcoholic drinks every day while using this
product

• take more or for a longer time than directed

Do not use:
• if you have ever had an allergic reaction to any
  other pain
• reliever/fever reducer
• right before or after heart surgery
• if you have ever had an allergic reaction to this
  product or any of its ingredients

Ask a doctor before use if:
• you have liver disease

Ask a doctor or pharmacist before use if you are:
• under a doctor’s care for any serious condition
• taking the blood thinning drug Warfarin

When using this product:
• take with food or milk if stomach upset occurs
• the risk of heart attack or stroke may increase if
  you use more than directed or for longer than
  directed

Stop use and ask a doctor if:
• pain gets worse lasts more than 10 days
• feel faint
• pain gets worse or lasts more than 10 days
• fever gets worse or lasts more than 3 days
• redness or swelling is present in the painful area
• any new symptoms occur

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

Keep out of reach of children. In case of overdose,
get medical help or contact a Poison Control Center
right away. Prompt medical attention is critical for
adults as well as for children even if you do not
notice any signs or symptoms.

Directions:
do not take more than directed
• adults and children 12 years and over: take 2
  tablets every 4 to 6 hours as needed
• do not exceed 8 tablets in 24 hours, unless
  directed by a doctor
• Children under 12 years: Do not use this product

Other information:
read all warnings and directions before use. Keep
carton. Store at 20-25°C (68-77°F) avoid excessive
heat above 40°C (104°F)

Inactive Ingredients:
Microcrystalline Cellulose, Povidone, Sodium Starch
Glycolate, Starch, Stearic Acid

Package Labeling

aramark

100 TABLETS        Part # 90433B
PER BOX

Extra Strength
Acetaminophen
Pain Reliever/Fever Reducer

Temporary relief of minor aches and
pains associated with a cold,
headache, tootache, muscular aches,
and for the reduction of fever

Compare active ingredient to:
Extra Strength Tylenol®
Registered Trademark of Johnson & Johnson

MANUFACTURED FOR:

Aramark
Lenexa, KS 66219
866-362-2691

aramarkuniform.com

Retain carton for complete product information

100 Tablet Box

100 ct 3500-1 Box

250 Tablet Box

250 ct 3500-2 Box

2-Tablet Packet

2ct 3500 Packet

res

ARAMARK EXTRA STRENGTH ACETAMINOPHEN 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81238-3500
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POVIDONE (UNII: FZ989GH94E)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize18mm
FlavorImprint Code FR1
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81238-3500-150 in 1 BOX05/14/2021
12 in 1 PACKET; Type 0: Not a Combination Product
2NDC:81238-3500-2125 in 1 BOX05/14/2021
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 finalpart34305/14/2021
Labeler - Western First Aid Safety DBA Aramark (043861524)
Registrant - Western First Aid Safety DBA Aramark (043861524)
Establishment
NameAddressID/FEIBusiness Operations
ULTRA SEAL CORPORATION085752004pack(81238-3500)
Establishment
NameAddressID/FEIBusiness Operations
ULTRA SEAL CORPORATION944090448manufacture(81238-3500)

Revised: 7/2021
Document Id: 1114224d-5c96-43e0-aa89-bb7b1550be47
Set id: 9bf4ca22-2546-4803-a199-b7d782e04a97
Version: 2
Effective Time: 20210719
 
Western First Aid Safety DBA Aramark