ALLERGY RELIEF- diphenhydramine hcl 25 mg tablet, film coated

Allergy Relief by

Drug Labeling and Warnings

Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Mechanical Servants, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Diphenhydramine HCl 25 mg

Purpose

Antihistamine

Uses

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

Warnings

Do not use

• to make a child sleepy
• with any other product containing diphenhydramine, even one used on skin

Ask a doctor before use if you have

• a breathing problem such as emphysema or chronic bronchitis
• glaucoma
• trouble urinating due to an enlarged prostate gland

Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives.

When using this product

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

• take every 4 to 6 hours, or as directed by a doctor
• do not take more than 6 doses in 24 hours

• adults and children 12 years and over: take 1 to 2 tablets
• children 6 to under 12 years: take 1 tablet
• children under 6 years: do not use

Other Information

• each tablet may contain: calcium 25 mg
• store at room temperature 68°-77°F (20°-25°C)
• protect from light and moisture

Inactive Ingredients

carnauba wax 1 , colloidal silicon dioxide, croscarmellose sodium, D&C red #27, dicalcium phosphate 1 , hypromellose, lactose 1 , magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80 1 , titanium dioxide

1 may contain

Questions or Comments

call toll-free 800-351-2000 (M-F 8:00 AM-4:30 PM CST)

SPL UNCLASSIFIED SECTION

* This product is not manufactured or distributed by

JOHNSON & JOHNSON CONSUMER INC,

McNeil Consumer Healthcare Division,

distributor of Benadryl® Allergy ULTRATABS®

Distributed by:

Lil’ Drug Store Products, Inc.

Cedar Rapids, IA 52404

PRINCIPAL DISPLAY PANEL

COMPARE TO THE ACTIVE INGREDIENTS IN

Benadryl® Allergy ULTRATABS®

Allergy Relief

Diphenhydramine HCl 25 mg,

Antihistamine

Relieves Symptoms of

Hay Fever, Common Cold and [tablet image here]

Other Upper Respiratory Allergies actual size

2 TABLETS IN EACH PACKET

INGREDIENTS AND APPEARANCE

ALLERGY RELIEF 
diphenhydramine hcl 25 mg tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 29485-9285
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M)	DIPHENHYDRAMINE HYDROCHLORIDE	25 mg

Inactive Ingredients
Ingredient Name	Strength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CARNAUBA WAX (UNII: R12CBM0EIZ)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
D&C RED NO. 27 (UNII: 2LRS185U6K)
ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	pink	Score	no score
Shape	OVAL	Size	11mm
Flavor		Imprint Code	048;D
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 29485-9285-2	25 in 1 BOX	07/11/2016	06/18/2027
1		2 in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 29485-9285-3	30 in 1 BOX	07/11/2016	03/28/2027
2		2 in 1 POUCH; Type 0: Not a Combination Product
3	NDC: 29485-9285-4	50 in 1 BOX	07/11/2016	06/24/2027
3		2 in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	07/11/2016	06/24/2027

Labeler - Lil' Drug Store Products, Inc. (093103646)