Childrens Allergy Relief

Manufacturer
AptaPharma Inc.
Effective date
2018-10-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:45:43

Label at a glance#

ProductChildrens Allergy Relief
Active ingredientDIPHENHYDRAMINE HYDROCHLORIDE
Label structure14 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each 5 mL)
Diphenhydramine HCl               12.5 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 the child has
• glaucoma
• abreathing problem such as chronic bronchitis

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if the child is taking
sedatives or tranquilizers

OTC - WHEN USING SECTION

When using this product

• marked drowsiness will occur
• excitability may occur, especially in children
• sedatives and tranquilizers may increase drowsiness

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
do not take more than 6 doses in 24 hours
mL= millilite

 Age                                                                Dose

children 6 to under 12 years

of age

5 mL to 10 mL

children 4 to under 6 years

of age

Do not use unless directed

by a doctor

children under 4 years of age

 Do not use

OTHER SAFETY INFORMATION

Other information
• each 5 mL contains: sodium 3 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 Children's
Benadryl® Allergy Liquid*

Children's
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
6 to 12 Years

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 Children's Benadryl®
Allergy Liquid.

Lot:
Exp:

LR-112 #194380

Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2018 CVS/pharmacy
CVS.com® 1-800-SHOP CVS
V-34801

√CVS Quality
Money Back Guarantee

Package Label

313-26 Label313-26 Label

                                           Children's Allergy Relief by CVS Pharmacy, Inc.

res

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76281-31376281-313-26

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

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
320efef0-2bde-4bc8-a071-faf048b658cc3608d7ac-c056-4c85-8ebc-4f54c73696292023-12-30WarningsExact identifier
spl set id: 3608d7ac-c056-4c85-8ebc-4f54c7369629

Reported adverse events (FAERS/openFDA)#

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