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Up and Up Acid Reducer

Pronunciation

Generic Name: ranitidine
Dosage Form: tablet

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Target Corp. Acid Reducer Drug Facts

Active ingredient (in each tablet)

Ranitidine 75 mg (as ranitidine hydrochloride 84 mg)

Purpose

Acid reducer

Uses

relieves heartburn associated with acid indigestion and sour stomach
prevents heartburn associated with acid indigestion and sour stomach brought on by eating or drinking certain foods and beverages

Warnings

Allergy alert: Do not use if you are allergic to ranitidine or other acid reducers

Do not use

if you have trouble or pain swallowing food, vomiting with blood, or bloody or black stools. These may be signs of a serious condition. See your doctor.
with other acid reducers

Ask a doctor before use if you have

frequent chest pain
frequent wheezing, particularly with heartburn
unexplained weight loss
nausea or vomiting
stomach pain
had heartburn over 3 months. This may be a sign of a more serious condition
heartburn with lightheadedness, sweating or dizziness
chest pain or shoulder pain with shortness of breath; sweating; pain spreading to arms, neck or shoulders; or lightheadedness

Stop use and ask a doctor if

your heartburn continues or worsens
you need to take this product for more than 14 days

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 and over:
to relieve symptoms, swallow 1 tablet with a glass of water
to prevent symptoms, swallow 1 tablet with a glass of water 30 to 60 minutes before eating food or drinking beverages that cause heartburn
can be used up to twice daily (do not take more than 2 tablets in 24 hours)
children under 12 years: ask a doctor

Other information

do not use if printed foil under cap is broken or missing
store at 20° - 25°C (68° - 77°F)
avoid excessive heat or humidity
this product is sugar free

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, diethyl phthalate, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, titanium dioxide.

Questions?

Call 1-800-910-6874

Principal Display Panel

Ranitidine Tablets, USP 75 mg

Acid Reducer

Non-Prescription Strength

Compare to active ingredient in Zantac 75®

Relieves and Prevents Heartburn Associated with Acid Indigestion and Sour Stomach

# Tablets {Replace "#" with number tablets in package}

# Doses {Replace "#" with number tablets in package}

Acid Reducer Carton

Up and Up Acid Reducer NON PRESCRIPTION STRENGTH
ranitidine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:11673-271
Route of Administration	ORAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
RANITIDINE HYDROCHLORIDE (RANITIDINE)	RANITIDINE	75 mg

Product Characteristics
Color	PINK	Score	no score
Shape	HEXAGON (6 sided)	Size	8mm
Flavor		Imprint Code	W;75
Contains

Packaging
#	Item Code	Package Description
1	NDC:11673-271-39	1 BOTTLE (BOTTLE) in 1 CARTON
1		30 TABLET (TABLET) in 1 BOTTLE
2	NDC:11673-271-27	1 BOTTLE (BOTTLE) in 1 CARTON
2		80 TABLET (TABLET) in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA076760	07/31/2009

Labeler - Target Corporation (006961700)

Revised: 07/2009

Target Corporation

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