ACID REDUCER- esomeprazole magnesium tablet 
Walgreens

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Esomeprazole Magnesium Delayed-Release Capsules 20 mg - Actavis

Drug Facts

Active ingredient (in each tablet)

Esomeprazole 20 mg
(*Each delayed-release tablet corresponds to 22.25 mg esomeprazole magnesium, USP (trihydrate))

Purpose

Acid reducer

Uses

Warnings

Allergy alert:

If an allergic reaction occurs, stop use and seek medical help right away.

Do not use if you have

These may be signs of a serious condition. See your doctor.

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

Stop use and ask a doctor if

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

            14-Day Course of Treatment
            •  
swallow 1 tablet with a glass of water before eating in the morning
            •   take every day for 14 days 
            •   do not take more than 1 tablet a day 
            •   swallow whole. Do not crush or chew tablets.
            •   do not use for more than 14 days unless directed by your doctor

            Repeated 14-Day Courses (if needed)
            •  
you may repeat a 14-day course every 4 months
            •   do not take for more than 14 days or more often than every 4 months unless directed by a doctor

Other information

Inactive ingredients

black iron oxide, colloidal silicon dioxide, crospovidone, hydroxypropyl cellulose, hypromellose, low substituted hydroxypropyl cellulose, magnesium stearate, methacrylic acid - ethyl acrylate copolymer dispersion, microcrystalline cellulose, mono- and di-glycerides, polyethylene glycol, polysorbate 80, propylene glycol, red iron oxide, shellac glaze, sodium lauryl sulfate, sodium stearyl fumarate, sugar spheres (corn starch and sucrose), talc, titanium dioxide, triethyl citrate and yellow iron oxide

Questions or comments?

Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal Display Panel

Compare to the active ingredient in Nexium® 24HR††

Esomeprazole Magnesium

DELAYED-RELEASE TABLETS, 20 mg* / ACID REDUCER

24 Hour Tablets

TABLETS

SEE NEW WARNING INFORMATION

††This product is not manufactured or distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC, distributor of Nexium® 24HR.

TAMPER EVIDENT: DO NOT USE IF SEAL UNDER BOTTLE CAP IS BROKEN OR MISSING

KEEP CARTON FOR COMPLETE WARNINGS AND IMPORTANT INFORMATION

DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

Package label

Treats frequent heartburn

WALGREENS Esomeprazole Magnesium Delayed-Release Tablets 20 mg* / Acid Reducer

ACID REDUCER 
esomeprazole magnesium tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9977
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ESOMEPRAZOLE MAGNESIUM (UNII: R6DXU4WAY9) (ESOMEPRAZOLE - UNII:N3PA6559FT) ESOMEPRAZOLE20 mg
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
GLYCERYL MONO AND DIPALMITOSTEARATE (UNII: KC98RO82HJ)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER (UNII: NX76LV5T8J)  
POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
SUCROSE (UNII: C151H8M554)  
STARCH, CORN (UNII: O8232NY3SJ)  
TALC (UNII: 7SEV7J4R1U)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
TRIETHYL CITRATE (UNII: 8Z96QXD6UM)  
CROSPOVIDONE (UNII: 2S7830E561)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
HYDROXYPROPYL CELLULOSE, LOW SUBSTITUTED (UNII: 2165RE0K14)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SHELLAC (UNII: 46N107B71O)  
SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Product Characteristics
Colorwhite (Pink) Scoreno score
ShapeOVALSize14mm
FlavorImprint Code EL
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-9977-141 in 1 CARTON11/04/2022
114 in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:0363-9977-423 in 1 CARTON11/04/2022
214 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21208811/04/2022
Labeler - Walgreens (008965063)

Revised: 8/2023
Document Id: 6a3e27a9-1987-420c-8a14-34f8e8a9cc75
Set id: 4f3c1d76-e1ba-4f85-9384-ed8f35fa6bc6
Version: 2
Effective Time: 20230810
 
Walgreens