Aramark Back Relief

Manufacturer
Western First Aid Safety DBA Aramark | ULTRA SEAL CORPORATION
Effective date
2021-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:03

Label at a glance#

ProductAramark Back Relief
Active ingredientACETAMINOPHEN, CAFFEINE, MAGNESIUM SALICYLATE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient (in each tablet)
Acetaminophen 250 mg
Cafeine 50mg
*Nonsteroidal anti-inflammatory drug
Magnesium Salicylate (NSAID) 290 mg

OTC - PURPOSE SECTION

Purpose
Acetaminophen ....Pain Reliever/Fever Reducer
Cafeine .........................................Adjuvent
*Nonsteroidal anti-inflammatory drug
Magnesium Salicylate (NSAID) ......Pain Reliever

INDICATIONS & USAGE SECTION

Uses:
Temporarily Relieves minor aches and pains
associated with: • back pain • muscular aches

WARNINGS SECTION

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: Saticylates (NSAIDs) may cause a severe
   allergic reaction which may include: • hives • shock
   • facial swelling • asthma (wheezing)

If a skin or allergic reaction occurs, stop use
and seek medical help right away.

Liver Warning: This product contains acetaminophen.
   Severe liver damage may occur if you take:
   • more than 8 tablets in 24 hours
   • with other drugs containing acetaminophen
  (prescription or nonprescription)
   • Ask a doctor or pharmacist before using with
  other drugs if you are not sure.
   • 3 or more alcoholic drinks every day while using
   this product.
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
   • for pain for more than 10 days or for fever for
     more than 3 days unless directed by a doctor
   • with any other product containing
     acetaminophen
   • right before or after heart surgery

Ask a 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

When using this product do not exceed the
recommended dose.

Caffeine warning: The recommended dose of this
product contains about as much caffeine as a cup of coffee.
Limit the use of careline-containing medications, foods, or
beverages while taking this product because too much careline
may cause nervousness, irritability, sleeplessness, and,
occasionally, rapid heartbeat.

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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 SECTION

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

2 tablets as
needed for pain
every 4 hours. Do
not exceed 8 tablets
in 24 hours or as
directed by a doctor.

• Children under
12 years:
Do not give to
children under 12 years
of age

OTHER SAFETY INFORMATION

Other Information:
• read all product information before using
• store at room temperature 59°-86°F (15°-30°C)
• avoid excessive heat and humidity
• tamper-evident sealed packets
• do not use any opened or torn packets

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
hypromellose, maltodextrin, microcrystalline
cellulose, polyethylene glycol, povidone,
starch 1551, stearic acid, titanium dioxide

Product Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

aramark

100 Tablets                        Part # 07333

Per Box

Back Relief

Pain Reliever/Fever Reducer

MANUFACTURED FOR:

Aramark
Lenexa, KS 66219
(866) 362-2691

aramarkuniform.com

Retain carton for complete product information

100 Tablet Box

1118 100 Tab Cartn1118 100 Tab Cartn

2-tablet Packet

1118 2 Ct Paket1118 2 Ct Paket

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
283274acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral TabletPSN1
283274acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral TabletSCD1
283274APAP 250 MG / Caffeine 50 MG / Magnesium Salicylate 290 MG Oral TabletSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAFFEINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7dea7767-9f52-b60a-5435-33cb9cc28baeProduct name420250124
6338270f-96cb-0ecb-6fbb-0a9bc78001f4Product name720250116
0ca83774-3f79-b837-5d6f-c210102f3bc8Product name620250114
41b814f3-0166-1c53-c9ef-a0794c7daf9dProduct name320221110
a590be26-846c-8659-a5a1-fb25907965dcProduct name220221110
2dc76302-91c0-4c35-ad78-99adfb049c4bProduct name120200603
e6065d4b-5ae1-476f-a40e-f2851cbb5d2bProduct name220180221
f212291f-05fe-9603-fc7e-bd73e38ce1e6Product name220161129
182f9ab4-4ab5-c449-200f-87ce2ce8e550Product name220151105
332e86c3-7875-ca6e-f934-2206d2b31996Product name120140508
56625fcc-aa34-9d30-d0e9-1c1beb37ea21Product name120140508
7dfac40f-a405-cd2e-7c06-3059ec0e1092Product name120140508
96c2be53-8e44-452d-56a2-d255b2f1af2dProduct name120140508
bf8bd5f7-495f-4022-2780-7ded7ea7ea44Product name120140508
d223c173-c39b-d764-47d4-d671d3088815Product name120140508
e01133ad-4dcd-c7f3-454b-2ff569ee160aProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81238-1118-12023-01-30C16284748780-1f386c649-cd58-0266-e053-dadaa90a7c1aAramark Back Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81238-1118-1Aramark Back Relief2 in 1 PACKETTABLET21
81238-1118-1Aramark Back Relief50 in 1 BOXTABLET501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81238-1118ARAMARK BACK RELIEF (MAGNESIUM SALICYLATE) TABLET [WESTERN FIRST AID SAFETY DBA ARAMARK]1Legacy NDC, 2 package rows20210626_f33bce45-d5b3-4787-a961-bc07b3452aa3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81238-111881238-1118-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
6e3d45b6-1cc4-4db7-8644-f002c544e77cf33bce45-d5b3-4787-a961-bc07b3452aa32021-06-24WarningsExact identifier
spl id: 6e3d45b6-1cc4-4db7-8644-f002c544e77c
spl set id: f33bce45-d5b3-4787-a961-bc07b3452aa3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.