Maximum Strength Adult Allergy Relief

Manufacturer
AptaPharma Inc.
Effective date
2019-01-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:34:30

Label at a glance#

ProductMaximum Strength Adult Allergy Relief
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE
Label structure15 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each 20 mL)
Diphenhydramine HCl               50 mg

OTC - PURPOSE SECTION

Purpose
Diphenhydramine HCl ............................. Antihistamine

INDICATIONS & USAGE SECTION

Uses
■ temporarily relieves these symptoms due to hay fever or
other respiratory allergies: • sneezing • itching of the nose or throat
• runny nose • itchy watery eyes ■ temporarily relieves these
symptoms due to the common cold: • sneezing • runny nose

WARNINGS SECTION

Warnings
Do not use
• with any other product containing diphenhydramine, even one
  used on skin
• to make a child sleepy

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have
• a breathing problem such as chronic bronchitis
• glaucoma
• trouble urinating due to enlarged prostate gland

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are taking
sedatives or tranquilizers

OTC - WHEN USING SECTION

When using this product
• marked drowsiness may occur
• avoid alcoholic drinks
• sedatives and tranquilizers may increase drowsiness
• be careful when driving a motor vehicle or operating machinery
• excitability may occur, especially in children

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. In case of overdose, get
medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions
• if needed, take every 4-6 hours, or as directed by a
  doctor
• do not take more than 6 doses in 24 hours
• not to exceed 300 mg in 24 hours
• mL=milliliter

Age                                                         Dose 
 adults and children

 12 years and older

  10 mL to 20 mL
 children under 12 years of age Consult a doctor

OTHER SAFETY INFORMATION

Other information
• each 20 mL contains: sodium 12 mg
• store at 20-25°C (68-77°F).
• dosage cup provided

INACTIVE INGREDIENT SECTION

Inactive ingredients

Anhydrous citric acid, flavor, purified water, sodium benzoate, sucrose

OTC - QUESTIONS SECTION

Questions? Call weekdays from 9:30 AM to 4:30 PM EST at 1-877-798-5944

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CVS
HealthTM

Compare to the
active ingredient in
Benadryl® Allergy*

MAXIMUM STRENGTH
Adult
ALLERGY RELIEF
LIQUID MEDICATION

Free of alcohol, dyes &
artificial sweeteners

DIPHENHYDRAMINE HCl
ORAL SOLUTION
Antihistamine

Relieves:
• Sneezing; Runny nose
• Itchy, watery eyes
• Itchy throat

Cherry Flavor

For Ages
12 and Over

8 FL OZ (237 mL)

  DO NOT USE IF IMPRINTED SHRINK BAND IS MISSING OR BROKEN
Failure to follow these warnings could result in serious consequences

*This product is not manufactured or distributed by McNeil
Consumer Healthcare, distributor of Benadryl®​ Allergy.

Lot:
Exp:

LR-118      #344121

0   50428 60619   3

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CVS AlrgyMaxStrngth -319CVS AlrgyMaxStrngth -319

                                           Maximum Strength Adult Allergy Relief by CVS Pharmacy, Inc.

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76281-31976281-319-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML · Source PDF

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
fd544d9c-973b-4374-92b9-8dca20cff6bb481a83d4-a927-4148-82cc-70e06f058ddb2023-12-30WarningsExact identifier
spl set id: 481a83d4-a927-4148-82cc-70e06f058ddb

Reported adverse events (FAERS/openFDA)#

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