ACID REDUCER REGULAR STRENGTH- ranitidine tablet, film coated
Kmart Corporation

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Smart Sense 44-619-Delisted

Active ingredient
(in each tablet)

Ranitidine 75 mg
(as ranitidine hydrochloride USP, 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 any 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 (1-800-222-1222) 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 minutesbefore 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

TAMPER EVIDENT: DO NOT USE IF THE CARTON OR INDIVIDUAL BLISTER UNIT IS OPEN OR TORN
store at 20º-25ºC (68º-77ºF)
avoid excessive heat or humidity
this product is sodium and sugar free
see end flap for expiration date and lot number

Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, hypromellose, iron oxide red, magnesium stearate, microcrystalline cellulose, polyethylene glycol 400, talc, titanium dioxide

Questions or comments?

1-800-842-7886

Principal display panel

NDC 49738-619-01

Compare to the active ingredient of Regular Strength Zantac 75®*

Smart sense™

ACID REDUCER
REGULAR STRENGTH
Ranitidine Tablets USP

75 mg ACID REDUCER

PREVENTS & RELIEVES HEARTBURN
Associated with Acid Indigestion
and Sour Stomach

30 TABLETS (30 doses)

TAMPER EVIDENT: DO NOT USE IF THE CARTON OR INDIVIDUAL BLISTER UNIT IS OPEN OR TORN

*This product is not manufactured or distributed by Boehringer Ingelheim Pharmaceuticals, Inc., owner of the registered trademark Zantac 75®.

Distributed by: Kmart Corporation
Hoffamn Estates, IL 60179
Shop kmart.com
Product of India

SATISFACTION GUARANTEE
Thank you for purchasing this quality product. If you are unsatisfied for any reason, return the unused portion to the store for a full refund or call 1-800-842-7886.

50844 ORG031361901

Smart Sense 44-619

ACID REDUCER REGULAR STRENGTH
ranitidine tablet, film coated

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49738-619
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
RANITIDINE HYDROCHLORIDE (UNII: BK76465IHM) (RANITIDINE - UNII:884KT10YB7)	RANITIDINE	75 mg

Ingredient Name	Strength
Inactive Ingredients
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
HYPROMELLOSES (UNII: 3NXW29V3WO)
FERRIC OXIDE RED (UNII: 1K09F3G675)
MAGNESIUM STEARATE (UNII: 70097M6I30)
TALC (UNII: 7SEV7J4R1U)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	PINK	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	OR;606
Contains

#	Item Code	Package Description
Packaging
1	NDC:49738-619-01	3 in 1 CARTON
1		10 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
ANDA	ANDA200536	06/15/2013	07/15/2018

Labeler - Kmart Corporation (008965873)

Name	Address	ID/FEI	Business Operations
Establishment
LNK International, Inc.		038154464	PACK(49738-619)

Name	Address	ID/FEI	Business Operations
Establishment
Shasun Pharmaceuticals Limited		915786829	API MANUFACTURE(49738-619)

Revised: 7/2015

Document Id: 0905203c-804b-4756-8272-d955cef5c299

Set id: 4ee90204-7b0e-4c99-bd09-aef522012793

Version: 3

Effective Time: 20150715

Kmart Corporation