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#
Contacts and useful links#
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: | 2 tablets as |
| • 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
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
2-tablet Packet
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | SPL version |
|---|---|---|---|
| 283274 | acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet | PSN | 1 |
| 283274 | acetaminophen 250 MG / caffeine 50 MG / magnesium salicylate 290 MG Oral Tablet | SCD | 1 |
| 283274 | APAP 250 MG / Caffeine 50 MG / Magnesium Salicylate 290 MG Oral Tablet | SY | 1 |
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| CAFFEINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7dea7767-9f52-b60a-5435-33cb9cc28bae | Product name | 4 | 20250124 |
| 6338270f-96cb-0ecb-6fbb-0a9bc78001f4 | Product name | 7 | 20250116 |
| 0ca83774-3f79-b837-5d6f-c210102f3bc8 | Product name | 6 | 20250114 |
| 41b814f3-0166-1c53-c9ef-a0794c7daf9d | Product name | 3 | 20221110 |
| a590be26-846c-8659-a5a1-fb25907965dc | Product name | 2 | 20221110 |
| 2dc76302-91c0-4c35-ad78-99adfb049c4b | Product name | 1 | 20200603 |
| e6065d4b-5ae1-476f-a40e-f2851cbb5d2b | Product name | 2 | 20180221 |
| f212291f-05fe-9603-fc7e-bd73e38ce1e6 | Product name | 2 | 20161129 |
| 182f9ab4-4ab5-c449-200f-87ce2ce8e550 | Product name | 2 | 20151105 |
| 332e86c3-7875-ca6e-f934-2206d2b31996 | Product name | 1 | 20140508 |
| 56625fcc-aa34-9d30-d0e9-1c1beb37ea21 | Product name | 1 | 20140508 |
| 7dfac40f-a405-cd2e-7c06-3059ec0e1092 | Product name | 1 | 20140508 |
| 96c2be53-8e44-452d-56a2-d255b2f1af2d | Product name | 1 | 20140508 |
| bf8bd5f7-495f-4022-2780-7ded7ea7ea44 | Product name | 1 | 20140508 |
| d223c173-c39b-d764-47d4-d671d3088815 | Product name | 1 | 20140508 |
| e01133ad-4dcd-c7f3-454b-2ff569ee160a | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81238-1118-1 | 2023-01-30 | C162847 | 48780-1 | f386c649-cd58-0266-e053-dadaa90a7c1a | Aramark Back Relief |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81238-1118-1 | Aramark Back Relief | 2 in 1 PACKET | TABLET | 2 | 1 | |
| 81238-1118-1 | Aramark Back Relief | 50 in 1 BOX | TABLET | 50 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81238-1118 | ARAMARK BACK RELIEF (MAGNESIUM SALICYLATE) TABLET [WESTERN FIRST AID SAFETY DBA ARAMARK] | 1 | Legacy NDC, 2 package rows | 20210626_f33bce45-d5b3-4787-a961-bc07b3452aa3.zip |
Products#
Every source-derived product name is available through these pages.
- Aramark Back Relief
- Magnesium Salicylate
- ACETAMINOPHEN
- CAFFEINE
- SALICYLIC ACID
- HYPROMELLOSE, UNSPECIFIED
- MALTODEXTRIN
- MICROCRYSTALLINE CELLULOSE
- POLYETHYLENE GLYCOL, UNSPECIFIED
- POVIDONE
- STARCH, CORN
- STEARIC ACID
- TITANIUM DIOXIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81238-1118 | 81238-1118-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| CAFFEINE | 3G6A5W338E | ACTIB |
| MAGNESIUM SALICYLATE | 41728CY7UX | ACTIB |
| HYPROMELLOSE, UNSPECIFIED | 3NXW29V3WO | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| POLYETHYLENE GLYCOL, UNSPECIFIED | 3WJQ0SDW1A | IACT |
| POVIDONE | FZ989GH94E | IACT |
| STARCH, CORN | O8232NY3SJ | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| TITANIUM DIOXIDE | 15FIX9V2JP | IACT |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 6e3d45b6-1cc4-4db7-8644-f002c544e77c | f33bce45-d5b3-4787-a961-bc07b3452aa3 | 2021-06-24 | Warnings | 6e3d45b6-1cc4-4db7-8644-f002c544e77c f33bce45-d5b3-4787-a961-bc07b3452aa3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.

