HELP I HAVE ALLERGIES- loratadine tablet

Help I have allergies by

Drug Labeling and Warnings

Help I have allergies by is a Otc medication manufactured, distributed, or labeled by Help Remedies, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                                 Purpose
(in each tablet)

Loratadine 10mg..........................................Antihistamine

PURPOSE

Use

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies

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

WARNINGS

Warnings

Do not use ifyou have ever had an allergic reaction to this product or any of its ingredients


Ask a doctor before use if you have

• liver or kidney disease
• your doctor should determine if you need a different dose

When using this product do not take more than directed.Taking more than directed may
cause drowsiness.

Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical
help right away.

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.

PREGNANCY OR BREAST FEEDING

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

DOSAGE & ADMINISTRATION

Directions

• adults and children 6 years and over: 1 tablet daily; not more than 1 tablet in 24 hours
• children under 6 years of age: ask a doctor
• consumers with liver or kidney disease: ask a doctor

INDICATIONS & USAGE

Other Information

• do not use if individual blister is open or torn
• store between 20-25 degrees celcius (68-77 degrees fahrenheits)
• protect from excessive moisture
• use by expiration date on package
• keep carton. They contain important information.
  

INACTIVE INGREDIENT

Inactive Ingredients

corn starch, lactose monohydrate, magnesium stearate,pregelatinized starch

QUESTIONS

Distributed by Help Remedies,
57 W. 28th St. Fl. 4
New York, NY 10001
www.helpineedhelp.com

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HELP I HAVE ALLERGIES 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49260-611
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Loratadine (UNII: 7AJO3BO7QN) (Loratadine - UNII:7AJO3BO7QN)	Loratadine	10 mg

Inactive Ingredients
Ingredient Name	Strength
STARCH, CORN (UNII: O8232NY3SJ)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND (round)	Size	7mm
Flavor		Imprint Code	RX526
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49260-611-24	24 in 1 BOTTLE
2	NDC: 49260-611-08	8 in 1 BLISTER PACK

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/01/2009

Labeler - Help Remedies, Inc. (050359682)