OMEPRAZOLE MAGNESIUM- omeprazole magnesium 20.6mg capsules capsule, delayed release 
Wal-Mart Stores Inc

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Active ingredient (in each capsule)

*Omeprazole delayed-release capsules 20 mg
(equivalent to 20.6 mg omeprazole magnesium)

Purpose

Acid reducer

Use

Warnings

Allergy alert:

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; sweating; 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 a prescription drug.

Acid reducers may interact with certain prescription drugs.

Stop use and ask a 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
  • you develop a rash or joint pain

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(1-800-222-1222).

Directions

Other information

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, sodium lauryl sulphate, sugar spheres, talc, titanium dioxide, triethyl citrate

Questions

1-888-287-1915

Tips for Managing Heartburn

Omeprazole Delayed-Release Capsules, 20 mg* 14-count - Carton Label

NDC 49035-397-52

equate™

Compare to
Prilosec OTC®

Active
Ingredient**

Omeprazole
Delayed-Release Capsules, 20mg*
Acid Reducer

Treats Frequent
Heartburn
Occuring 2 or More
Days a Week

One 14-day couse
of treatment

20 mg 14 CAPSULES SAFETY SEALED

carton


Omeprazole Delayed-Release Capsules, 20 mg* 14-count - Bottle Label

equate™ NDC 49035-397-52

Omeprazole
Delayed-Release Capsules, 20mg*
Acid Reducer


Treats Frequent Heartburn
Occuring 2 or More Days a Week
One 14-day couse  of treatment

One 14-day course of
treatment (14 Capsules) 20 mg

Label

OMEPRAZOLE MAGNESIUM 
omeprazole magnesium 20.6mg capsules capsule, delayed release
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-397(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:49035-397-521 in 1 CARTON01/15/2010
114 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:49035-397-272 in 1 CARTON01/15/2010
214 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:49035-397-333 in 1 CARTON01/15/2010
314 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07887801/15/2010
Labeler - Wal-Mart Stores Inc (051957769)

Revised: 10/2023
Document Id: 7e7066c4-ccf9-1dae-8b40-a076df63879f
Set id: 3160e212-9ee9-8316-f51e-4628862f654c
Version: 5
Effective Time: 20231015
 
Wal-Mart Stores Inc