cimetidine

Manufacturer
Walgreen Company
Effective date
2025-03-10
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 00:57:12

Label at a glance#

Productcimetidine 200 acid reducer
Active ingredientCIMETIDINE
Label structure9 sections

Indications and 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

Dosage and administration

• 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 right before or any time up to 30 minutes before eating food or drinking beverages that cause heartburn • do not take more than 2 tablets in 24 hours • children under 12 years: ask a doctor

Storage and handling

• store at 20°-25°C (68°-77°F)

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Cimetidine 200 mg

Purpose

OTC - PURPOSE SECTION

Acid reducer

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

Allergy alert: Do not use if you are allergic to cimetidine or other acid reducers

Do not use

OTC - DO NOT USE SECTION

  • 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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

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

Ask a doctor or pharmacist before use if you are taking

OTC - ASK DOCTOR/PHARMACIST SECTION

  • a prescription drug. Acid reducers may interact with certain prescription drugs.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you need to take this product for more than 14 days
  • stomach pain continues
  • your heartburn continues or worsens

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 right before or any time up to 30 minutes before eating food or drinking beverages that cause heartburn
    • do not take more than 2 tablets in 24 hours
  • children under 12 years: ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • store at 20°-25°C (68°-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, pregelatinized starch, sodium lauryl sulfate, sodium starch glycolate, titanium dioxide

Questions or comments?

OTC - QUESTIONS SECTION

1-800-719-9260

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

WALGREENS PHARMACIST RECOMMENDED

Compare to the active ingredient in Tagamet® HB 200

Cimetidine 200

CIMETIDINE TABLETS USP, 200 mg / ACID REDUCER

● Just one tablet relieves & prevents heartburn & acid indigestion

● Take before, during or after a meal

60 TABLETS (60 DOSES)

ACTUAL SIZE

cimetidine-200-carton-image-1
cimetidine-200-carton-image-1
cimetidine-200-carton-image-2
cimetidine-200-carton-image-2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
197505cimetidine 200 MG Oral TabletPSN8
197505cimetidine 200 MG Oral TabletSCD8

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
8f48ba86-02a3-4def-9efa-3a8140fd7adfProduct name220250624

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0022-72cimetidine 200acid reducer60 in 1 BOTTLETABLET, FILM COATED608
0363-0022-72cimetidine 200acid reducer1 in 1 CARTONTABLET, FILM COATED18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0022CIMETIDINE 200 ACID REDUCER (CIMETIDINE) TABLET, FILM COATED [WALGREEN COMPANY]8Current NDC, Legacy NDC, 2 package rows20250316_7087f4bb-992b-4680-a9a7-452ce74eed2d.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0022-72EA - Each0363-0022f74dde83-3860-453e-a79c-df6c045c3fea12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CIMETIDINEACTIVE INGREDIENT80061L1WGD2
CIMETIDINEACTIVE MOIETY80061L1WGD2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WO2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I302
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1A2
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8H2
POVIDONESINACTIVE INGREDIENTFZ989GH94E2
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141J2
SODIUM STARCH GLYCOLATE TYPE A POTATOINACTIVE INGREDIENT5856J3G2A22
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJ2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JP2

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-00220363-0022-72

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 16 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
POVIDONESPOVIDONEFZ989GH94ETABLET, FILM COATED / ORAL240 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
POVIDONESPOVIDONEFZ989GH94ETABLET, FILM COATED / ORAL240 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, FILM COATED / ORAL36 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, FILM COATED / ORAL240 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET, FILM COATED / ORAL96 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET, FILM COATED / ORAL96 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED / ORAL992 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED / ORAL992 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
HYPROMELLOSESHYPROMELLOSE3NXW29V3WOTABLET, FILM COATED / ORAL582 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
SODIUM LAURYL SULFATESODIUM LAURYL SULFATE368GB5141JTABLET, FILM COATED / ORAL240 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, FILM COATED / ORAL36 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
POLYSORBATE 80POLYSORBATE 806OZP39ZG8HTABLET, FILM COATED / ORAL24 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, FILM COATED / ORAL2000 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
POLYSORBATE 80POLYSORBATE 806OZP39ZG8HTABLET, FILM COATED / ORAL24 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
STARCH, CORNSTARCH, CORNO8232NY3SJTABLET, FILM COATED / ORAL2000 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
HYPROMELLOSESHYPROMELLOSE3NXW29V3WOTABLET, FILM COATED / ORAL582 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates

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 43.

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
A075285-001CIMETIDINECIMETIDINE200MGTABLET / ORAL1998-10-29

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.

Product history page 1 of 2 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-2984e616aacf4f…
2026-08-18 06:07:402026-07A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-2931067a03dcf5…
2025-08-23 18:47 UTC2025-08A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-296a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-2903ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-292680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-295bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-2979d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-291e350fbaab3a…
2024-05-31 18:47 UTC2024-05A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-298072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-295c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-295d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-294b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-2974a2ff9319b5…
2022-03-09 01:35 UTC2022-03A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-2987673890dc5c…
2021-03-12 10:30 UTC2021-03A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-295aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-298869cabd3fbd…
2020-11-12 02:37 UTC2020-11A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29c0c555d07b60…
2019-12-14 00:12 UTC2019-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-293f01610625f2…
2019-09-15 20:21 UTC2019-09A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29b00525d2431f…
2019-07-19 19:46 UTC2019-07A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-296a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-291c564ffb4f44…
2023-12-20 04:57 UTC2023-12A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-299b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-293f0d92c62455…
2023-05-13 08:27 UTC2023-05A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29053a50430f4f…
2023-01-26 05:58 UTC2023-01A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-293bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-293a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A075285-001CIMETIDINE200MGTABLET / ORAL1998-10-29f41ea6bd6efb…

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
cimetidine 200 acid reducerCIMETIDINEWalgreen Company7087f4bb-992b-4680-a9a7-452ce74eed2d2025-03-10WarningsExact identifier
ndc (package): 0363-0022-72
ndc (product): 0363-0022
ndc11 (package): 00363002272
spl id: 84970421-ebbc-45ad-a5ca-58038d3bf539
spl set id: 7087f4bb-992b-4680-a9a7-452ce74eed2d

Reported adverse events (FAERS/openFDA)#

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