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#

ProductMaximum Allergy Relief
Active ingredientACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
Label structure15 sections

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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

0140-1 100ct Box0140-1 100ct Box

250 Tablet Box

0140-2 250ct Box0140-2 250ct Box

2-Tablet Packet

0140 2ct Pouch0140 2ct Pouch

res

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1101534acetaminophen 500 MG / phenylephrine HCl 5 MG Oral TabletPSN1
1101534acetaminophen 500 MG / phenylephrine hydrochloride 5 MG Oral TabletSCD1
1101534APAP 500 MG / Phenylephrine Hydrochloride 5 MG Oral TabletSY1

DailyMed Pharmacologic Classes#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81238-0240-12023-01-30C16284748780-1f386c64a-3ef5-0266-e053-dadaa90a7c1aAramark Maximum Allergy Relief
81238-0240-22023-01-30C16284748780-1f386c64a-3ef5-0266-e053-dadaa90a7c1aAramark Maximum Allergy Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81238-0240-1Maximum Allergy Relief50 in 1 BOXTABLET501
81238-0240-1Maximum Allergy Relief2 in 1 PACKETTABLET21
81238-0240-2Maximum Allergy Relief125 in 1 BOXTABLET1251
81238-0240-2Maximum Allergy Relief2 in 1 PACKETTABLET21

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81238-0240MAXIMUM ALLERGY RELIEF (ACETAMINOPHEN, PHENYLEPHRINE HCL) TABLET [WESTERN FIRST AID SAFETY DBA ARAMARK]1Legacy NDC, 4 package rows20210613_cabd4342-7957-42ad-baa3-1f6c512cdf8c.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81238-024081238-0240-1, 81238-0240-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
6e3cc529-336b-4c7c-a635-0fdbf5f14967cabd4342-7957-42ad-baa3-1f6c512cdf8c2021-06-11WarningsExact identifier
spl id: 6e3cc529-336b-4c7c-a635-0fdbf5f14967
spl set id: cabd4342-7957-42ad-baa3-1f6c512cdf8c

Reported adverse events (FAERS/openFDA)#

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