acid reducer

Manufacturer
Publix Super Markets Inc
Effective date
2025-02-17
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:55:35

Label at a glance#

Productacid reducer
Active ingredientFAMOTIDINE
Label structure8 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 food and beverages

Dosage and administration

• adults and children 12 years and over: • to relieve symptoms, swallow 1 tablet with a glass of water. Do not chew. • to prevent symptoms, swallow 1 tablet with a glass of water at any time from 15 to 60 minutes before eating food or drinking beverages that cause heartburn • do not use more than 2 tablets in 24 hours • children under 12 years: ask a doctor

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Famotidine 10 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 food and beverages

Warnings

WARNINGS SECTION

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

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

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

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. Do not chew.
  • to prevent symptoms, swallow 1 tablet with a glass of water at any time from 15 to 60 minutes before eating food or drinking beverages that cause heartburn
  • do not use more than 2 tablets in 24 hours
  • children under 12 years: ask a doctor

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

carnauba wax, hypromellose, iron oxide red, iron oxide yellow, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, pregelatinized starch, talc, titanium dioxide, triacetin

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FAMOTIDINE TABLETS, 10 mg

acid reducer

ORIGINAL STRENGTH

ACTUAL SIZE

• Just one tablet prevents and relieves heartburn due to acid indigestion

30 TABLETS

Compare to Pepcid® AC Original Strength active ingredient

SEE NEW WARNINGS

141-63-acid-reducer
141-63-acid-reducer

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199047famotidine 10 MG Oral TabletPSN5
199047famotidine 10 MG Oral TabletSCD5

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
396bde5c-c78e-2f8b-ab1f-2ee6ba32bcaeProduct name720260317
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
cf645750-2e70-f6e1-c05a-a52847def5ddProduct name920250312
4fdc761c-585e-054b-8ebe-86130a26e4c1Product name220221205
fc2e1e31-353a-2c24-a4b4-fcf93bf7e38eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
56062-141-65acid reducer30 in 1 CARTONTABLET, FILM COATED305
56062-141-65acid reducer1 in 1 BLISTER PACKTABLET, FILM COATED15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
56062-141ACID REDUCER (FAMOTIDINE) TABLET, FILM COATED [PUBLIX SUPER MARKETS INC]5Current NDC, Legacy NDC, 2 package rows20250221_a3ba9983-6747-45b2-b270-4ac1fb9d6e40.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
56062-141-65EA - Each56062-141c3af4a18-45d1-42a8-82bc-147421b1c30e12022-06-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
FAMOTIDINEACTIVE INGREDIENT5QZO15J2Z82
FAMOTIDINEACTIVE MOIETY5QZO15J2Z82
CARNAUBA WAXINACTIVE INGREDIENTR12CBM0EIZ2
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61U2
FERRIC OXIDE REDINACTIVE INGREDIENT1K09F3G6752
FERRIC OXIDE YELLOWINACTIVE INGREDIENTEX438O2MRT2
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WO2
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I302
POLYDEXTROSEINACTIVE INGREDIENTVH2XOU12IE2
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1A2
TALCINACTIVE INGREDIENT7SEV7J4R1U2
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JP2
TRIACETININACTIVE INGREDIENTXHX3C3X6732

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
56062-14156062-141-65

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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 · 20 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
MAGNESIUM STEARATEMAGNESIUM STEARATE70097M6I30TABLET, FILM COATED / ORAL96 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TRIACETINTRIACETINXHX3C3X673TABLET, FILM COATED / ORAL15.12 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
FERRIC OXIDE YELLOWFERRIC OXIDE YELLOWEX438O2MRTTABLET, FILM COATED / ORAL6 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
POLYDEXTROSEPOLYDEXTROSEVH2XOU12IETABLET, FILM COATED / ORAL18 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
FERRIC OXIDE REDFERRIC OXIDE RED1K09F3G675TABLET, FILM COATED / ORAL3 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
CARNAUBA WAXCARNAUBA WAXR12CBM0EIZTABLET, FILM COATED / ORAL1 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, FILM COATED / ORAL91 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TALCTALC7SEV7J4R1UTABLET, FILM COATED / ORAL91 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
CARNAUBA WAXCARNAUBA WAXR12CBM0EIZTABLET, FILM COATED / ORAL1 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
FERRIC OXIDE REDFERRIC OXIDE RED1K09F3G675TABLET, FILM COATED / ORAL3 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
TITANIUM DIOXIDETITANIUM DIOXIDE15FIX9V2JPTABLET, FILM COATED / ORAL36 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
TRIACETINTRIACETINXHX3C3X673TABLET, FILM COATED / ORAL15.12 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
CELLULOSE, MICROCRYSTALLINEMICROCRYSTALLINE CELLULOSEOP1R32D61UTABLET, FILM COATED / ORAL992 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
FERRIC OXIDE YELLOWFERRIC OXIDE YELLOWEX438O2MRTTABLET, FILM COATED / ORAL6 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
POLYDEXTROSEPOLYDEXTROSEVH2XOU12IETABLET, FILM COATED / ORAL18 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 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
A075400-001FAMOTIDINEFAMOTIDINE10MGTABLET / ORAL2005-03-18

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 · 44 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-10-15 13:18:302026-09A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18c2088c7a36db…
2026-09-14 22:38:342026-08A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-1884e616aacf4f…
2026-08-18 06:07:402026-07A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-1831067a03dcf5…
2025-08-23 18:47 UTC2025-08A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-186a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-1803ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-182680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-185bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-1879d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-181e350fbaab3a…
2024-05-31 18:47 UTC2024-05A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-188072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-185c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-185d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-184b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-1874a2ff9319b5…
2022-03-09 01:35 UTC2022-03A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-1887673890dc5c…
2021-03-12 10:30 UTC2021-03A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-185aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-188869cabd3fbd…
2020-11-12 02:37 UTC2020-11A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18c0c555d07b60…
2019-12-14 00:12 UTC2019-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-183f01610625f2…
2019-09-15 20:21 UTC2019-09A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18b00525d2431f…
2019-07-19 19:46 UTC2019-07A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-186a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-181c564ffb4f44…
2023-12-20 04:57 UTC2023-12A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-189b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-183f0d92c62455…
2023-05-13 08:27 UTC2023-05A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-18053a50430f4f…
2023-01-26 05:58 UTC2023-01A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-183bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A075400-001FAMOTIDINE10MGTABLET / ORAL2005-03-183a93d1ddd44b…

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
acid reducerFAMOTIDINEPublix Super Markets Inca3ba9983-6747-45b2-b270-4ac1fb9d6e402025-02-17WarningsExact identifier
ndc (package): 56062-141-65
ndc (product): 56062-141
ndc11 (package): 56062014165
spl id: edd72fec-0dfc-4862-8d07-476e74b2fe69
spl set id: a3ba9983-6747-45b2-b270-4ac1fb9d6e40

Reported adverse events (FAERS/openFDA)#

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