Esomeprazole Magnesium Delayed-Release Capsules USP, 20 mg (OTC)

Manufacturer
MARKSANS PHARMA LIMITED
Effective date
2026-06-01
Label type
Human OTC Drug Label
Version
3
Source
daily-update
Hydrated at
2026-06-03 18:04:06

Label at a glance#

ProductEsomeprazole Magnesium Delayed-Release 20 mg (OTC)
Active ingredientESOMEPRAZOLE MAGNESIUM
Label structure14 sections

Dosage and administration

Directions adults 18 years of age and older this product is to be used once a day (every 24 hours), every day for 14 days may take 1 to 4 days for full effect   14-Day Course of Treatment swallow 1 capsule with a glass of water before eating in the morning take every day for 14 days do not take more than 1 capsule a day swallow whole. Do not crush or chew capsules. do not use for more than 14 days unless directed ...

Storage and handling

Other information read the directions and warnings before use keep the carton. It contains important information. store at 20-25°C (68-77°F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each capsule) 
Esomeprazole 20 mg
(Each delayed-release capsule corresponds to 22.3 mg 
 esomeprazole magnesium trihydrate)



PURPOSE

OTC - PURPOSE SECTION

Purpose 
Acid reducer








USE(S)

INDICATIONS & USAGE SECTION

Uses

  • treats frequent heartburn (occurs 2 or more days a week)
  • not intended for immediate relief of heartburn; this drug may take 1 to 4 days for full effect

WARNINGS

WARNINGS SECTION

Allergy alert:

  • Do not use if you are allergic to esomeprazole
  • Esomeprazole may cause severe skin reactions. Symptoms include:
    • skin reddening 
    • blisters
    • rash

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


DO NOT USE

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

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

OTC - ASK DOCTOR/PHARMACIST SECTION

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 DOCTOR IF

OTC - STOP USE SECTION

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

PREGNANCY/BREASTFEEDING

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults 18 years of age and older
  • this product is to be used once a day (every 24 hours), every day for 14 days
  • may take 1 to 4 days for full effect

 

14-Day Course of Treatment

  • swallow 1 capsule with a glass of water before eating in the morning
  • take every day for 14 days
  • do not take more than 1 capsule a day
  • swallow whole. Do not crush or chew capsules.
  • 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
  •  children under 18 years of age: ask a doctor before use. Heartburn in children may sometimes be caused by a serious condition.

STORAGE

STORAGE AND HANDLING SECTION

Other information

  • read the directions and warnings before use
  • keep the carton. It contains important information.
  • store at 20-25°C (68-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

 

Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg

 

Inactive ingredients black iron oxide, D&C red 28, eudragit, FD&C blue 1, FD&C red 40, ferric oxide yellow, gelatin, glyceryl monostearate, hydroxypropyl cellulose, hypromellose, magnesium stearate, polysorbate 80, potassium hydroxide, shellac, simethicone, sodium lauryl sulfate, sugar spheres, talc, titanium dioxide, triethyl citrate.


Esomeprazole Magnesium Delayed-Release Capsules 20 mg (Mini Capsules)

 

Inactive ingredients black iron oxide, corn starch, D&C red 27 aluminum lake, D&C red no. 28, eudragit, FD&C blue 1, FD&C red no. 40, ferric oxide yellow, gelatin, glyceryl monostearate, hydroxypropyl cellulose, hypromellose, magnesium stearate, polysorbate 80, potassium hydroxide, shellac, simethicone, sodium lauryl sulfate, sucrose, talc, titanium dioxide, triethyl citrate.

 

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 25000-088-76

Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg (OTC)

14 count bottle label


esomeprazole-otc-dr-20mg-14s-bottle-label
esomeprazole-otc-dr-20mg-14s-bottle-label


NDC: 25000-088-76

Esomeprazole Magnesium Delayed-Release Capsules USP 20 mg (OTC)

14 count carton label


esomeprazole-otc-dr-20mg-14s-cartonesomeprazole-otc-dr-20mg-14s-carton

NDC: 25000-096-76
Esomeprazole Magnesium Delayed-Release Capsules 20 mg (Mini capsules)

14 count bottle label

esomeprazole-otc-dr-minis-20mg-14s-bottle-labelesomeprazole-otc-dr-minis-20mg-14s-bottle-label

 

NDC: 25000-096-76
Esomeprazole Magnesium Delayed-Release Capsules 20 mg (Mini capsules)

14 count carton label

 

esomeprazole-otc-dr-minis-20mg-14s-cartonesomeprazole-otc-dr-minis-20mg-14s-carton




DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ESOMEPRAZOLE Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130325000088767GTIN-13: 0325000088767
EAN-13: 0325000088767
GTIN-12: 325000088767
UPC-A: 325000088767
GTIN storage (14 digits): 00325000088767
esomeprazole-otc-dr-20mg-14s-carton.jpg
BarcodeEAN-130325000096762GTIN-13: 0325000096762
EAN-13: 0325000096762
GTIN-12: 325000096762
UPC-A: 325000096762
GTIN storage (14 digits): 00325000096762
esomeprazole-otc-dr-minis-20mg-14s-carton.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d7006a36-e68d-42e2-8cd3-d725cb2e47b1Product name620251027
d71865e8-5c35-4d76-8ecd-a7adda982240Product name920180628
d71865e8-5c35-4d76-8ecd-a7adda982240Product name820171212
094c6751-235c-4d12-acee-2baf94f676f4Product name120151116
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
25000-08825000-088-76
25000-09625000-096-76

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 2 · 45 matching rows.

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
A217264-001ESOMEPRAZOLE MAGNESIUMESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-10-15 13:18:302026-09A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29c2088c7a36db…
2026-09-14 22:38:342026-08A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-2984e616aacf4f…
2026-08-18 06:07:402026-07A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-2931067a03dcf5…
2025-08-23 18:47 UTC2025-08A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-296a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-2903ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-292680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-295bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-2979d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-291e350fbaab3a…
2024-05-31 18:47 UTC2024-05A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-298072bd15b7f6…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-296a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-291c564ffb4f44…
2023-12-20 04:57 UTC2023-12A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-299b2671bbb829…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06A217264-001ESOMEPRAZOLE MAGNESIUMEQ 20MG BASECAPSULE, DELAYED RELEASE / ORAL2023-09-29a50c72e98297…

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Esomeprazole Magnesium Delayed-Release 20 mg (OTC)ESOMEPRAZOLE MAGNESIUM DELAYED-RELEASE 20 MG (OTC)MARKSANS PHARMA LIMITED6a21f085-b60b-49b7-8098-99ccdc43dde32026-06-01WarningsExact identifier
ndc (package): 25000-088-76
ndc (package): 25000-096-76
ndc (product): 25000-096
ndc (product): 25000-088
ndc11 (package): 25000008876
ndc11 (package): 25000009676
spl id: f2f3282e-c6de-42ea-9a6f-d6b573256968
spl set id: 6a21f085-b60b-49b7-8098-99ccdc43dde3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.