AMAZON BASIC CARE NAPROXEN SODIUM

Manufacturer
Amazon.com Services LLC | Aurohealth LLC | Aurobindo Pharma Limited
Effective date
2025-05-26
Label type
Human OTC Drug Label
Version
3
Source
full-release
Hydrated at
2026-06-01 01:01:33

Label at a glance#

ProductAMAZON BASIC CARE NAPROXEN SODIUM
Active ingredientNAPROXEN SODIUM
Label structure18 sections

Indications and uses

temporarily relieves minor aches and pains due to: headache minor pain of arthritis muscular aches backache menstrual cramps toothache the common cold temporarily reduces fever

Dosage and administration

do not take more than directed the smallest effective dose should be used drink a full glass of water with each dose  Adults and children  12 years and older take 1 tablet every 8 to 12 hours while symptoms last for the first dose you may take 2 tablets within the first hour do not exceed 2 tablets in any 8 to 12 hour period do not exceed 3 tablets in a 24 hour period   Children under 12 years  ask a doctor

Storage and handling

each tablet contains: sodium 20 mg store at 20° to 25°C (68° to 77°F). Avoid high humidity and excessive heat above 40°C (104°F).

Label contents#

Full prescribing information#

Naproxen Sodium Tablets, USP 220 mg

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Naproxen sodium USP 220 mg (naproxen 200 mg) (NSAID)*

*nonsteroidal anti-inflammatory drug

Purposes

OTC - PURPOSE SECTION

Pain reliever/fever reducer

Uses

INDICATIONS & USAGE SECTION

  • temporarily relieves minor aches and pains due to:
  • headache
  • minor pain of arthritis
  • muscular aches
  • backache
  • menstrual cramps
  • toothache
  • the common cold
  • temporarily reduces fever

Warnings

WARNINGS SECTION

Allergy alert: Naproxen sodium may cause a severe allergic reaction, especially in people allergic to aspirin. Symptoms may include:


  • hives
  • facial swelling
  • asthma (wheezing)
  • shock
  • skin reddening
  • rash
  • blisters

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

Stomach bleeding warning:
This product contains an NSAID, which may cause severe stomach bleeding. The chance is higher if you:


  • are age 60 or older
  • have had stomach ulcers or bleeding problems
  • take a blood thinning (anticoagulant) or steroid drug
  • take other drugs containing prescription or nonprescription NSAIDs (aspirin, ibuprofen, naproxen, or others)
  • have 3 or more alcoholic drinks every day while using this product
  • take more or for a longer time than directed

Heart attack and stroke warning: NSAIDs, except aspirin, increase the risk of heart attack, heart failure, and stroke. These can be fatal. The risk is higher if you use more than directed or for longer than directed.

Do not use

OTC - DO NOT USE SECTION

  • if you have ever had an allergic reaction to any other pain reliever/fever reducer
  • right before or after heart surgery

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

  • the stomach bleeding warning applies to you
  • you have a history of stomach problems, such as heartburn
  • you have high blood pressure, heart disease, liver cirrhosis, kidney disease, asthma, or had a stroke
  • you are taking a diuretic
  • you have problems or serious side effects from taking pain relievers or fever reducers

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • under a doctor's care for any serious condition
  • taking aspirin for heart attack or stroke, because naproxen may decrease this benefit of aspirin
  • taking any other drug

When using this product

OTC - WHEN USING SECTION

  • take with food or milk if stomach upset occurs

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • you experience any of the following signs of stomach bleeding:
    • feel faint
    • vomit blood
    • have bloody or black stools
    • have stomach pain that does not get better
  • you have symptoms of heart problems or stroke:
    • chest pain
    • trouble breathing
    • weakness in one part or side of body
    • slurred speech
    • leg swelling
  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • you have difficulty swallowing
  • it feels like the pill is stuck in your throat
  • redness or swelling is present in the painful area
  • any new symptoms appear

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use. It is especially important not to use naproxen sodium at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • do not take more than directed
  • the smallest effective dose should be used
  • drink a full glass of water with each dose

 Adults and children
 12 years and older
  • take 1 tablet every 8 to 12 hours while symptoms last
  • for the first dose you may take 2 tablets within the first hour
  • do not exceed 2 tablets in any 8 to 12 hour period
  • do not exceed 3 tablets in a 24 hour period
 Children under 12 years
 ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • each tablet contains: sodium 20 mg
  • store at 20° to 25°C (68° to 77°F). Avoid high humidity and excessive heat above 40°C (104°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

colloidal silicon dioxide, FD&C blue #2 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, povidone, talc, and titanium dioxide

Questions or comments?

OTC - QUESTIONS SECTION

1-855-274-4122

DISTRIBUTED BY: AMAZON.COM SERVICES LLC
410 TERRY AVENUE N., SEATTLE, WA 98109
© 2024 AMAZON.COM, INC. OR ITS AFFILIATES.
ALL RIGHTS RESERVED.

Made in India

***This product is not Manufactured or
distributed by Bayer Healthcare LLC,
distributor of Aleve®.



PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (90 Tablets, Container Label)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

amazon

basic+care

Strength to Last 12 Hours

NDC 72288-366-90

Naproxen
Sodium
Tablets USP 220 mg
(NSAID)

Pain Reliever/Fever Reducer

90 TABLETS

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (90 Tablets, Container Label)PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (90 Tablets, Container Label)

PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (90 Tablets Container Carton Label)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

amazon

basic+care

Strength to
Last 12 Hours

Compare to
Aleve®
active
ingredient***

NDC 72288-366-90

Naproxen
Sodium
Tablets USP 220 mg
(NSAID)

Pain Reliever/
Fever Reducer

90 TABLETS
PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (90 Tablets Container Carton Label)PACKAGE LABEL-PRINCIPAL DISPLAY PANEL - 220 mg (90 Tablets Container Carton Label)

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
849574naproxen sodium 220 MG Oral TabletPSN3
849574naproxen sodium 220 MG Oral TabletSCD3
849574naproxen sodium 220 MG (as naproxen 200 MG) Oral TabletSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
NAPROXEN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20191108

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fef6ad89-235f-4274-ba49-a8e53642473eProduct name220250225
594e2c86-3079-4e6e-96c9-48f7a8afc78dProduct name120230718
87fed3e6-8fba-48ef-96b0-3a7fb54b96ffProduct name320230306
b5fdaaec-7251-4da6-9cb2-4e9e76939ec8Product name120200623
e76dbbc1-775d-722c-08ff-ed45e8a80defProduct name320181002
6f4f4521-fd56-1ae6-888b-3b021bd75c7cProduct name120140508
ce67e27d-1d21-5465-4409-b0662dd99d4dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72288-366-20AMAZON BASIC CARE NAPROXEN SODIUM200 in 1 BOTTLETABLET, FILM COATED2003
72288-366-20AMAZON BASIC CARE NAPROXEN SODIUM1 in 1 CARTONTABLET, FILM COATED13
72288-366-30AMAZON BASIC CARE NAPROXEN SODIUM300 in 1 BOTTLETABLET, FILM COATED3003
72288-366-30AMAZON BASIC CARE NAPROXEN SODIUM1 in 1 CARTONTABLET, FILM COATED13
72288-366-90AMAZON BASIC CARE NAPROXEN SODIUM1 in 1 CARTONTABLET, FILM COATED13
72288-366-90AMAZON BASIC CARE NAPROXEN SODIUM90 in 1 BOTTLETABLET, FILM COATED903

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72288-366AMAZON BASIC CARE NAPROXEN SODIUM (NAPROXEN SODIUM) TABLET, FILM COATED [AMAZON.COM SERVICES LLC]3Current NDC, 6 package rows20250528_10ee5bc0-509d-b549-e063-6394a90a5dca.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72288-36672288-366-90, 72288-366-20, 72288-366-30

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

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
A205497-001NAPROXEN SODIUMNAPROXEN SODIUM220MGTABLET / ORAL2016-03-18

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 · 43 observed states.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1884e616aacf4f…
2026-08-18 06:07:402026-07A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18caaa826d4ba7…
2026-02-19 14:30 UTC2026-02A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1831067a03dcf5…
2025-08-23 18:47 UTC2025-08A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-186a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18b8a1b40f171c…
2025-01-19 17:59 UTC · 7 captures of this ZIP2025-01A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1803ed91905a0d…
2024-12-13 21:23 UTC · 2 captures of this ZIP2024-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-182680178bc6a6…
2024-09-14 05:58 UTC · 2 captures of this ZIP2024-09A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185bbf6a4d5a75…
2024-11-08 22:44 UTC · 3 captures of this ZIP2024-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18d8e5a09893c0…
2024-10-29 15:01 UTC2024-10A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18d06236e962d9…
2024-08-13 05:28 UTC · 3 captures of this ZIP2024-08A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1879d66fd596c7…
2024-07-13 05:37 UTC · 2 captures of this ZIP2024-07A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18301d65b070ca…
2024-06-18 03:08 UTC · 5 captures of this ZIP2024-06A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-181e350fbaab3a…
2024-05-31 18:47 UTC2024-05A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-188072bd15b7f6…
2022-06-29 02:47 UTC · 2 captures of this ZIP2022-06A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185c6f7cd8ea54…
2022-04-08 23:34 UTC2022-04A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185d02ea3f76ae…
2022-04-04 05:41 UTC2022-04A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-184b0b4de00fa7…
2019-12-13 00:20 UTC2019-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1874a2ff9319b5…
2022-03-09 01:35 UTC2022-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18bb7c543d1eb4…
2021-12-28 21:50 UTC2021-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18782e0a99824c…
2021-05-05 16:15 UTC · 3 captures of this ZIP2021-05A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-1887673890dc5c…
2021-03-12 10:30 UTC2021-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-185aa47cf7b7d7…
2020-12-22 03:56 UTC2020-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-188869cabd3fbd…
2020-11-12 02:37 UTC2020-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18c0c555d07b60…
2019-12-14 00:12 UTC2019-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183f01610625f2…
2019-09-15 20:21 UTC2019-09A205497-001NAPROXEN SODIUMEQ 200MG BASETABLET / ORAL2016-03-18b00525d2431f…
2019-07-19 19:46 UTC2019-07A205497-001NAPROXEN SODIUMEQ 200MG BASETABLET / ORAL2016-03-18ea99ee380514…
2024-03-16 18:09 UTC · 4 captures of this ZIP2024-03A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-186a51e52b5d6a…
2024-02-18 07:12 UTC2024-02A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-181c564ffb4f44…
2023-12-20 04:57 UTC2023-12A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18ea1830bbd6c7…
2023-11-28 05:40 UTC · 2 captures of this ZIP2023-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18a72a2bbeb626…
2023-10-25 00:34 UTC · 2 captures of this ZIP2023-10A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-189b2671bbb829…
2023-07-15 15:27 UTC · 2 captures of this ZIP2023-07A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18a67488948f0b…
2023-06-13 01:57 UTC · 3 captures of this ZIP2023-06A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183f0d92c62455…
2023-05-13 08:27 UTC2023-05A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18053a50430f4f…
2023-01-26 05:58 UTC2023-01A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183bdfa0b2c4d7…
2022-11-12 20:34 UTC · 5 captures of this ZIP2022-11A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-183a93d1ddd44b…
2022-10-28 04:53 UTC2022-10A205497-001NAPROXEN SODIUM220MGTABLET / ORAL2016-03-18f41ea6bd6efb…

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
AMAZON BASIC CARE NAPROXEN SODIUMNAPROXEN SODIUMAmazon.com Services LLC10ee5bc0-509d-b549-e063-6394a90a5dca2025-05-26WarningsExact identifier
ndc (package): 72288-366-90
ndc (package): 72288-366-20
ndc (package): 72288-366-30
ndc (product): 72288-366
ndc11 (package): 72288036620
ndc11 (package): 72288036630
ndc11 (package): 72288036690
spl id: 0931d3d1-7ac4-4076-865e-a8ba9e295bc8
spl set id: 10ee5bc0-509d-b549-e063-6394a90a5dca

Reported adverse events (FAERS/openFDA)#

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