MAXIMUM STRENGTH ADULT ALLERGY RELIEF- diphenhydramine hcl liquid

Maximum Strength Adult Allergy Relief by

Drug Labeling and Warnings

Maximum Strength Adult Allergy Relief by is a Otc medication manufactured, distributed, or labeled by AptaPharma Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

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

PURPOSE

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

INDICATIONS & USAGE

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

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

ASK DOCTOR

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

ASK DOCTOR/PHARMACIST

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

WHEN USING

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

PREGNANCY OR BREAST FEEDING

If pregnant or breast feeding, ask a health professional before use

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

Inactive ingredients

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

QUESTIONS

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

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INGREDIENTS AND APPEARANCE

MAXIMUM STRENGTH ADULT ALLERGY RELIEF 
diphenhydramine hcl liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76281-319
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	50 mg  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76281-319-26	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	11/01/2018

Labeler - AptaPharma Inc. (790523323)

Registrant - AptaPharma Inc. (790523323)

Establishment
Name	Address	ID/FEI	Business Operations
AptaPharma Inc.		790523323	manufacture(76281-319)