Maximum Allergy Relief
- Manufacturer
- Western First Aid Safety DBA Aramark | ULTRA SEAL CORPORATION
- Effective date
- 2021-06-11
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:40:48
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Drug Facts
Active Ingredient (in each tablet)
Acetaminophen 500 mg
Phenylephrine HLC 5 mg
OTC - PURPOSE SECTION
Purpose
Acetaminophen ...................Pain reliever/fever reducer
Phenylephrine HLC ................Nasal decongestant
INDICATIONS & USAGE SECTION
Uses:
Temporarily relieves these symptoms
associated with hay fever or other
respiratory allergies and the common cold:
• headache • sinus congestion and pressure
• nasal congestion • minor aches and pains
• promotes sinus drainage
• temporarily reduces fever
WARNINGS SECTION
Warnings:
Liver warning: This product contains acetaminophen.
The maximum daily dose of this product is 6 tablets
(3,000 mg acetaminophen) in 24 hours. Severe liver
damage may occur if you take:
•more than 4,000 mg of acetaminophen in 24 hours
•with other drugs containing acetaminophen
•3 or more alcoholic drinks every day while using this
product
Allergy alert: acetaminophen may cause serve skin
reactions. Symptoms may include:
•skin reddening •blister •rash
If a skin reaction occurs, stop use and seek medical
help right away
OTC - DO NOT USE SECTION
Do not use
•with any other drug containing acetaminophen. If
you are not sure whether a drug contains
acetaminophen, ask a doctor or pharmacist.
•if you are now taking a prescription monoamine
oxidase inhibitor (MAOIs), or for 2 weeks after
stopping the MAOI drug. If you do not know if
your prescription drug contains an MAOI, ask a
doctor or pharmacist before taking this product.
•if you have ever had an allergic reaction to this
product or any of its ingredients.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if you have:
• liver disease
• diabetes
• heart disease
• high blood pressure
• thyroid disease
• trouble urinating due to an enlarged prostate
gland
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are
taking the blood thinning drug Warfarin
OTC - WHEN USING SECTION
When using this product do not exceed
recommended dose
OTC - STOP USE SECTION
Stop use and ask a doctor if:
• nervousness, dizziness, or sleeplessness occur
• pain or nasal congestion gets worse or lasts
more than 7 days
• fever gets worse or lasts more than 3 days
• redness or swelling is present
• new symptoms occur
These could be signs of a serious condition.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health
professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
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.
DOSAGE & ADMINISTRATION SECTION
Directions:
• do not take more than directed (see
overdose warning)
• adults and children 12 years and over:
• take 2 tablet every 4 hours
• swallow whole; do not crush, chew or
dissolve
• do not take more than 6 tablets in 24
hours
• children under 12 years: ask a doctor
OTHER SAFETY INFORMATION
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 INGREDIENT SECTION
Inactive Ingredients:
Corn Starch, FD & C Blue #1 Lake, Microcystalline
Cellulose, Povidone, Sodium Starch Glycolate,
Stearic Acid, USP Purified Water
Package Labeling
aramark
100 TABLETS Part # 91933B
PER BOX
Maximum
Allergy Relief
Pain Reliever/Nasal Decongestant
Temporary relief of headaches,
sinus pain, nasal and sinus congestion,
minor aches, pains, fever
MANUFACTURED FOR:
Aramark
Lenexa, KS 66219
(913) 269-9611
aramarkuniform.com
Retain carton for complete product information
100 Tablet Box
250 Tablet Box
2-Tablet Packet
res
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| PHENYLEPHRINE Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 81238-0240-1 | 2023-01-30 | C162847 | 48780-1 | f386c64a-3ef5-0266-e053-dadaa90a7c1a | Aramark Maximum Allergy Relief |
| 81238-0240-2 | 2023-01-30 | C162847 | 48780-1 | f386c64a-3ef5-0266-e053-dadaa90a7c1a | Aramark Maximum Allergy Relief |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81238-0240-1 | Maximum Allergy Relief | 50 in 1 BOX | TABLET | 50 | 1 | |
| 81238-0240-1 | Maximum Allergy Relief | 2 in 1 PACKET | TABLET | 2 | 1 | |
| 81238-0240-2 | Maximum Allergy Relief | 125 in 1 BOX | TABLET | 125 | 1 | |
| 81238-0240-2 | Maximum Allergy Relief | 2 in 1 PACKET | TABLET | 2 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 81238-0240 | MAXIMUM ALLERGY RELIEF (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET [WESTERN FIRST AID SAFETY DBA ARAMARK] | 1 | Legacy NDC, 4 package rows | 20210613_cabd4342-7957-42ad-baa3-1f6c512cdf8c.zip |
Products#
Every source-derived product name is available through these pages.
- Maximum Allergy Relief
- ACETAMINOPHEN, PHENYLEPHRINE HCl
- ACETAMINOPHEN
- PHENYLEPHRINE HYDROCHLORIDE
- PHENYLEPHRINE
- STARCH, CORN
- FD&C BLUE NO. 1
- MICROCRYSTALLINE CELLULOSE
- POVIDONE
- SODIUM STARCH GLYCOLATE TYPE A CORN
- STEARIC ACID
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 81238-0240 | 81238-0240-1, 81238-0240-2 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| PHENYLEPHRINE HYDROCHLORIDE | 04JA59TNSJ | ACTIM |
| STARCH, CORN | O8232NY3SJ | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| POVIDONE | FZ989GH94E | IACT |
| SODIUM STARCH GLYCOLATE TYPE A CORN | AG9B65PV6B | IACT |
| STEARIC ACID | 4ELV7Z65AP | IACT |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| 6e3cc529-336b-4c7c-a635-0fdbf5f14967 | cabd4342-7957-42ad-baa3-1f6c512cdf8c | 2021-06-11 | Warnings | 6e3cc529-336b-4c7c-a635-0fdbf5f14967 cabd4342-7957-42ad-baa3-1f6c512cdf8c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.


