OMEPRAZOLE MAGNESIUM- omeprazole magnesium capsule, delayed release 
Meijer Distribution Inc

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Active ingredient

Omeprazole magnesium delayed-release capsule 20.6 mg

(equivalent to 20 mg omeprazole)

Purpose

Acid reducer

Use(s)

Warnings

Allergy alert: Do not use if you are allergic to omeprazole 

Do not use

if you have:

  • trouble or pain swallowing food, vomiting with blood, or bloody or black stools
  • heartburn with lightheadedness, sweating or dizziness
  • chest pain or shoulder pain with shortness of breath; pain spreading to arms, neck or shoulders; or lightheadedness
  • frequent chest pain
These may be signs of a serious condition. See your Doctor.

Ask a doctor before use if you have

    • had heartburn over 3 months. This may be a sign of a more serious condition

    • frequent wheezing, particularly with heartburn

    • unexplained weight loss

    • nausea or vomiting

    • stomach pain

Ask a doctor or pharmacist before use if

you are taking

  • warfarin, clopidogrel or cilostazol (blood-thinning medicines)
  • prescription antifungal or anti-yeast medicines
  • diazepam (anxiety medicine)
  • digoxin (heart medicine)
  • tacrolimus or mycophenolate mofetil (immune system medicines)
  • prescription antiretrovirals (medicines for HIV infection)
  • methotrexate (arthritis medicine)

Stop use and ask doctor if

  • your heartburn continues or worsens
  • you need to take this product for more than 14 days
  • you need to take more than 1 course of treatment every 4 months
  • you get diarrhea

Pregnancy/Breastfeeding

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

Other information

Storage

Inactive ingredients

black iron oxide, dibasic calcium phosphate, gelatin, glyceryl monostearate, hypromellose 3 cps, magnesium oxide, magnesium stearate, methacrylic acid copolymer dispersion, methacrylic acid copolymer Type B, microcrystalline cellulose, polysorbate 80, potassium hydroxide, propylene glycol, red iron oxide, shellac, silicon dioxide, sugar spheres, talc, titanium dioxide, triethyl citrate

Questions

Call 1-888-375-3784

Tips for Managing Heartburn

Principal Display Panel

Containercarton42 Omeprazole Magnesium Delayed-Release Capsules, 20. 6 mg - Container Label:

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OMEPRAZOLE MAGNESIUM 
omeprazole magnesium capsule, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-064(NDC:55111-397)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Omeprazole Magnesium (UNII: 426QFE7XLK) (omeprazole - UNII:KG60484QX9) omeprazole20 mg
Inactive Ingredients
Ingredient NameStrength
Ferrosoferric Oxide (UNII: XM0M87F357)  
Anhydrous Dibasic Calcium Phosphate (UNII: L11K75P92J)  
Gelatin (UNII: 2G86QN327L)  
Glyceryl Monostearate (UNII: 230OU9XXE4)  
Hypromellose 2208 (3 Mpa.S) (UNII: 9H4L916OBU)  
Magnesium Oxide (UNII: 3A3U0GI71G)  
Magnesium Stearate (UNII: 70097M6I30)  
Methacrylic Acid - Methyl Methacrylate Copolymer (1:2) (UNII: 5KY68S2577)  
Methacrylic Acid - Ethyl Acrylate Copolymer (1:1) Type A (UNII: NX76LV5T8J)  
Cellulose, Microcrystalline (UNII: OP1R32D61U)  
Polysorbate 80 (UNII: 6OZP39ZG8H)  
Potassium Hydroxide (UNII: WZH3C48M4T)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
SHELLAC (UNII: 46N107B71O)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
RAW SUGAR (UNII: 8M707QY5GH)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
Sodium Lauryl Sulfate (UNII: 368GB5141J)  
Product Characteristics
ColorWHITE, PINKScoreno score
ShapeCAPSULESize22mm
FlavorImprint Code OMP20
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41250-064-333 in 1 CARTON09/22/2014
1NDC:41250-064-5214 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07887809/22/2014
Labeler - Meijer Distribution Inc (006959555)

Revised: 12/2017
Document Id: 7e5c4f4f-4ef5-156b-3236-94459e5747ce
Set id: 1379897d-f4f9-4dac-73d1-9a7d5b6093c3
Version: 3
Effective Time: 20171207
 
Meijer Distribution Inc