482R_Albertson_21130-428_Aspirin Delayed -Release Tablets USP, 81mg EC
- Manufacturer
- BETTER LIVING BRANDS LLC. | TIME CAP LABORATORIES, INC.
- Effective date
- 2025-02-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-06-01 00:54:59
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient (in each tablet)
Aspirin 81 mg (NSAID)*
*nonsteroidal anti-inflammatory drug
OTC - PURPOSE SECTION
Purpose
Pain reliever
INDICATIONS & USAGE SECTION
Uses
• temporarily relieves minor aches and pain
• ask your doctor about other uses for enteric coated 81 mg Aspirin.
WARNINGS SECTION
Warnings
Reye’s syndrome: Children and teenagers who have or are recovering from chicken pox or flu-like symptoms should not use this product. When using this product, if changes in behavior with nausea and vomiting occur, consult a doctor because these symptoms could be an early sign of Reye’s syndrome, a rare but serious illness.
Allergy alert: Aspirin may cause a severe allergic reaction which may include:•hives • facial swelling • asthma (wheezing) • shock
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 problem
- 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
OTC - DO NOT USE SECTION
Do not use if you are allergic to aspirin or any other pain reliever/fever reducer
OTC - ASK DOCTOR SECTION
Ask a doctor before use if
- 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, or kidney disease
- you are taking a diuretic
- you have asthma
OTC - ASK DOCTOR/PHARMACIST SECTION
Ask a doctor or pharmacist before use if you are taking a prescription drug for gout, diabetes or arthritis
OTC - STOP USE SECTION
Stop use and ask a doctor if
- an allergic reaction occurs. Seek medical help right away.
- 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
- pain gets worse or lasts more than 10 days
- ringing in the ears or a loss of hearing occurs
- redness or swelling is present
- new symptoms occur
These could be signs of a serious condition.
PREGNANCY SECTION
If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use aspirin during the last 3 months of pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.
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.
DOSAGE & ADMINISTRATION SECTION
Directions
- drink a full glass of water with each dose
- adults and children 12 years of age and over: take 4 to 8 tablets every 4 hours not to exceed 48 tablets in 24 hours unless directed by a doctor
- children under 12 years of age: do not use unless directed by a doctor
OTHER SAFETY INFORMATION
Other information
- store at 20-25°C (68-77°F)
- close cap tightly after use
INACTIVE INGREDIENT SECTION
Inactive ingredients anhydrous lactose, carnauba wax, colloidal silicon dioxide, croscarmellose sodium, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, iron oxide yellow, methacrylic acid and ethyl acrylate copolymer, microcrystalline cellulose, polysorbate 80, simethicone, sodium hydroxide, sodium lauryl sulfate, starch, talc, triethyl citrate
OTC - QUESTIONS SECTION
Questions or comments?1-877-290-4008
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| ASPIRIN Pharmacologic Class Indexing | 3 | Indexing - Pharmacologic Class | 20191108 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| d7724692-1155-4cc8-a415-22f5fc4aec35 | Product name | 6 | 20220216 |
| bde672ba-4805-28d0-1986-73543d41b412 | Product name | 2 | 20210201 |
| f212291f-05fe-9603-fc7e-bd73e38ce1e6 | Product name | 2 | 20161129 |
| ade821ba-260a-47e2-bd89-743e27ac9906 | Product name | 1 | 20161121 |
| 182f9ab4-4ab5-c449-200f-87ce2ce8e550 | Product name | 2 | 20151105 |
| 9425d234-4ae1-4b53-adc6-8cc7af6dd657 | Product name | 1 | 20150929 |
| 2a21311a-89e2-0e83-2ebd-117f9798b2b2 | Product name | 1 | 20140508 |
| 9007e8a7-ff50-f9b9-7945-f2a1deadd94e | Product name | 1 | 20140508 |
| 96c2be53-8e44-452d-56a2-d255b2f1af2d | Product name | 1 | 20140508 |
| bf8bd5f7-495f-4022-2780-7ded7ea7ea44 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 21130-428-12 | 2025-02-11 | C162847 | 48780-1 | 2cef2736-9328-d83d-e063-dadaa90ab31f | 482R_Albertson_21130-428_Aspirin Delayed -Release Tablets USP, 81mg EC |
| 21130-428-20 | 2025-02-11 | C162847 | 48780-1 | 2cef2736-9328-d83d-e063-dadaa90ab31f | 482R_Albertson_21130-428_Aspirin Delayed -Release Tablets USP, 81mg EC |
| 21130-428-12 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9328-d83d-e063-dadaa90ab31f | 482R_Albertson_21130-428_Aspirin Delayed -Release Tablets USP, 81mg EC |
| 21130-428-20 | 2025-01-30 | C162847 | 48780-1 | 2cef2736-9328-d83d-e063-dadaa90ab31f | 482R_Albertson_21130-428_Aspirin Delayed -Release Tablets USP, 81mg EC |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 21130-428-12 | Aspirin 81mg | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | 3 | |
| 21130-428-12 | Aspirin 81mg | 120 in 1 BOTTLE | TABLET, DELAYED RELEASE | 120 | 3 | |
| 21130-428-20 | Aspirin 81mg | 200 in 1 BOTTLE | TABLET, DELAYED RELEASE | 200 | 3 | |
| 21130-428-20 | Aspirin 81mg | 1 in 1 CARTON | TABLET, DELAYED RELEASE | 1 | 3 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Aspirin 81mg
- Aspirin
- STARCH, CORN
- ANHYDROUS LACTOSE
- CARNAUBA WAX
- FD&C RED NO. 40 ALUMINUM LAKE
- SODIUM HYDROXIDE
- SILICON DIOXIDE
- CROSCARMELLOSE SODIUM
- POLYSORBATE 80
- TALC
- FD&C YELLOW NO. 6 ALUMINUM LAKE
- FERRIC OXIDE YELLOW
- DIMETHICONE
- SODIUM LAURYL SULFATE
- MICROCRYSTALLINE CELLULOSE
- METHACRYLIC ACID AND ETHYL ACRYLATE COPOLYMER
- TRIETHYL CITRATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 21130-428 | 21130-428-12, 21130-428-20 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Aspirin 81mg | ASPIRIN | BETTER LIVING BRANDS LLC. | f300dfbc-7137-79d1-e053-2995a90a636e | 2025-02-05 | Warnings | 21130-428-20 21130-428-12 21130-428 21130042820 21130042812 2d62fa1e-80f4-1f9e-e063-6394a90a575d f300dfbc-7137-79d1-e053-2995a90a636e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.



