ZANTAC 150 ACID REDUCER- ranitidine tablet 
Lil' Drug Store Products, Inc

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Zantac 150 ®

Acid Reducer

Drug Facts

Active ingredient (in each tablet)

Ranitidine 150 mg (as ranitidine hydrochloride 168 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
  • if you have kidney disease, except under the advice and supervision of a doctor

Ask a doctor before use if you have

  • 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
  • frequent chest pain
  • frequent wheezing, particularly with heartburn
  • unexplained weight loss
  • nausea or vomiting
  • stomach pain

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 healthcare 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 individual foil pouch is open or torn
  • store at 20°-25°C (68°-77°F)
  • avoid excessive heat or humidity
  • this product is sodium and sugar free

Inactive ingredients

hypromellose, magnesium stearate, microcrystalline cellulose, synthetic red iron oxide, titanium dioxide, triacetin

Questions?

call 1-800-633-1610 or visit www.zantacotc.com

Product repackaged and distributed by:
Lil' Drug Store Products, Inc.
9300 Earhart Lane SW, Cedar Rapids, IA 52404

PRINCIPAL DISPLAY PANEL - 150 mg Tablet Pouch Carton

MAXIMUM STRENGTH
Zantac
Ranitidine Tablets 150 mg/Acid Reducer
150 ®

PREVENTS & RELIEVES
HEARTBURN associated with
acid indigestion and sour stomach

3 Tablets
(3 Doses)

Lil'
Drug Store ®

Principal Display Panel - 150 mg Tablet Pouch Carton
ZANTAC 150  ACID REDUCER
ranitidine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-9736
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
RANITIDINE HYDROCHLORIDE (UNII: BK76465IHM) (RANITIDINE - UNII:884KT10YB7) RANITIDINE150 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIACETIN (UNII: XHX3C3X673)  
Product Characteristics
ColorbrownScoreno score
ShapePENTAGON (5 sided)Size4mm
FlavorImprint Code Z;150
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-9736-22 in 1 CARTON11/01/201011/01/2022
11 in 1 POUCH; Type 0: Not a Combination Product
2NDC:66715-9736-33 in 1 CARTON11/01/201011/01/2022
21 in 1 POUCH; Type 0: Not a Combination Product
3NDC:66715-9736-85 in 1 CARTON11/01/201011/01/2022
31 in 1 POUCH; Type 0: Not a Combination Product
4NDC:66715-9736-620 in 1 CARTON11/01/201012/31/2017
41 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02169811/01/201011/01/2022
Labeler - Lil' Drug Store Products, Inc (093103646)

Revised: 12/2020
Document Id: b595216b-d636-7f28-e053-2a95a90a40bc
Set id: 5e569962-0763-4669-96c2-93012ff6cd6c
Version: 6
Effective Time: 20201203
 
Lil' Drug Store Products, Inc