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Allergy Relief

CVS Pharmacy

CVS Pharmacy, Inc. Allergy Relief Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Clemastine fumarate, USP 1.34 mg (equivalent to 1 mg clemastine)

Purpose

Antihistamine

Allergy Relief Uses

temporarily reduces these symptoms of the common cold, hay fever, and other respiratory allergies:

  • runny nose
  • itchy, watery eyes
  • sneezing
  • itching of the nose or throat

Warnings

Ask a doctor before use if you have

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

Ask a doctor or pharmacist before use if you are

taking sedatives or tranquilizers

When using this product

  • avoid alcoholic drinks
  • drowsiness may occur
  • 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.

Directions

  • adults and children 12 years of age and over: take 1 tablet every 12 hours; not more than 2 tablets in 24 hours unless directed by a doctor
  • children under 12 years of age: consult a doctor

Allergy Relief Other information

  • sodium free
  • store at 15°-30°C (59°-86°F)

Inactive ingredients

colloidal silicon dioxide, lactose monohydrate, povidone, pregelatinized starch, starch, stearic acid

Questions or comments?

1-800-719-9260

Principal Display Panel

Compare to the active ingredient in Tavist® Allergy

ALLERGY RELIEF

CLEMASTINE FUMARATE TABLETS, USP 1.34 mg

ANTIHISTAMINE (CLEMASTINE FUMARATE)

12 Hour Relief

Runny Nose

Sneezing

Itchy, Watery Eyes

Itchy Throat

Allergy Relief
Allergy Relief Carton Image 1 Allergy Relief Carton Image 2

Allergy Relief

Clemastine fumarate TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:59779-282
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CLEMASTINE FUMARATE CLEMASTINE 1.34 mg

Inactive Ingredients

Ingredient Name Strength
SILICON DIOXIDE
lactose monohydrate
povidone
STEARIC ACID

Product Characteristics

Color Size Imprint Code Shape
WHITE (off white) 9 mm L282 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 8 in 1 BLISTER PACK
2 NDC:59779-282-73 2 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074512 1996-08-28


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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