ARAMARK ASPIRIN- aspirin tablet

Aramark Aspirin by

Drug Labeling and Warnings

Aramark Aspirin by is a Otc medication manufactured, distributed, or labeled by Western First Aid Safety DBA Aramark, Ultra Seal Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

(in Each Tablet)

Aspirin USP (NSAID)*  325 mg

*nonsteroidal anti-inflammatory drug

PURPOSE

Purpose
Pain Reliever/Fever Reducer

INDICATIONS & USAGE

Uses: temporarily relieves minor pain
due to: headache menstrual pain
minor pain of arthritis muscle pain
pain and fever of colds toothache
temporarily reduces fever

WARNINGS

Warnings:
Reye’s Syndrome: Children and teenagers
should not use this medicine for chicken pox or
flu symptoms before a doctor is consulted about
Reye’s Syndrome, a rare but serious illness
reported to be associated with aspirin

Allergy Alert - Do not use:
if you are allergic to aspirin or any other
  salicylate
if you have ever had an allergic reaction to any
  other pain reliever/fever reducer

Stomach Bleeding Warning:
This product contains nonsteroidal
anti-inflammatory drugs (NSAIDs), which may
cause stomach bleeding.

The chance is higher if you:
are age 60 or older
have had stomach ulcers or bleeding problems
take a blood thinning (anticoagulant) or
  steroid drug
take other drugs containing an NSAID
  (aspirin, ibuprofen, naproxen, or others)
take more or for a longer time than directed

Do not use:
with any other pain reliever/fever reducer

Ask doctor before using if you have:
upset stomach or stomach pain
ulcers
bleeding problems
high blood pressure
heart or kidney disease
taken a diuretic
reached age 60 or older

Ask a doctor or pharmacist before use if you are:
taking any other drug containing an NSAID
  (prescription or nonprescription) taking a blood
  thinning (anticoagulant) or steroid drug

Stop use and ask a doctor if: ringing in the
ears or loss of hearing occurs
pain or fever persists or gets worse
new symptoms occur
redness or swelling is present
you feel faint, vomit blood, or have bloody or
  black stools. These are signs of stomach
  bleeding.

If pregnant or breast-feeding baby, ask a health
professional before use. IT IS ESPECIALLY
IMPORTANT NOT TO USE ASPIRIN DURING
THE LAST 3 MONTHS OF PREGNANCY UNLESS
SPECIFICALLY DIRECTED TO DO SO BY A
DOCTOR BECAUSE IT MAY CAUSE PROBLEMS
IN THE UNBORN CHILD OR COMPLICATIONS
DURING DELIVERY.

KEEP OUT OF REACH OF CHILDREN

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 children even if you do not notice any
signs or symptoms.

DOSAGE & ADMINISTRATION

• Directions: Adults and children 12 years of age and older:

  Take 2 tablets every 4; to 6 hours as needed.; Do not exceed 12 tablets; in 24 hours or as directed; by a doctor.

• Children under 12 years: Consult a doctor.

INACTIVE INGREDIENT

Inactive Ingredients: FD&C Yellow #6,
Magnesium Stearate, Microcrystalline
Cellulose, Povidone, Starch, Stearic Acid

Product Package

aramark

Aspirin

Part # 556R23

100 TABLETS PER BOX

Compare active ingredient to:
BAYER®
Registered Trademark of Bayer Corp.

Retain carton for complete product information

MANUFACTURED FOR:
Aramark
Lenexa, KS 66219
(913) 269-9611

Box

Packet

res

INGREDIENTS AND APPEARANCE

ARAMARK ASPIRIN 
aspirin tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81238-0232
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASPIRIN (UNII: R16CO5Y76E) (ASPIRIN - UNII:R16CO5Y76E)	ASPIRIN	325 mg

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
MAGNESIUM STEARATE (UNII: 70097M6I30)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
POVIDONE (UNII: FZ989GH94E)
STARCH, CORN (UNII: O8232NY3SJ)
STEARIC ACID (UNII: 4ELV7Z65AP)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	FR21
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81238-0232-2	50 in 1 BOX	05/01/2021
1		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 not final	part343	05/01/2021

Labeler - Western First Aid Safety DBA Aramark (043861524)

Registrant - Western First Aid Safety DBA Aramark (043861524)

Establishment
Name	Address	ID/FEI	Business Operations
Ultra Seal Corporation		085752004	pack(81238-0232)

Establishment
Name	Address	ID/FEI	Business Operations
Ultra Seal Corporation		944090448	manufacture(81238-0232)