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#
Contacts and useful links#
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
| 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
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
DRUG FACTS →
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Maximum Strength Adult Allergy Relief by CVS Pharmacy, Inc.
res
Products#
Every source-derived product name is available through these pages.
- Maximum Strength Adult Allergy Relief
- DIPHENHYDRAMINE HCl
- DIPHENHYDRAMINE HYDROCHLORIDE
- DIPHENHYDRAMINE
- ANHYDROUS CITRIC ACID
- WATER
- SODIUM BENZOATE
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76281-319 | 76281-319-26 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | TC2D6JAD40 | ACTIB |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| WATER | 059QF0KO0R | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SUCROSE | C151H8M554 | 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 |
|---|---|---|---|---|---|---|
| fd544d9c-973b-4374-92b9-8dca20cff6bb | 481a83d4-a927-4148-82cc-70e06f058ddb | 2023-12-30 | Warnings | 481a83d4-a927-4148-82cc-70e06f058ddb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
