Redicare Non-Aspirin 500mg
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Redicare Non-Aspirin 500mg
- Generic name
- REDICARE NON-ASPIRIN, ACETAMINOPHEN 500MG
- Manufacturer
- Redicare LLC
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 2f229898-1777-732c-e063-6394a90a76bc
- SPL ID
- 2f850cc1-2c48-a305-e063-6294a90a40c7
- Version
- 2
- Effective date
- 2025-03-04
- Source export date
- 2026-09-28
- Source partition
- 5
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:33:37
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M013 | openfda.application_number | |
| brand name | Redicare Non-Aspirin 500mg | openfda.brand_name | |
| generic name | REDICARE NON-ASPIRIN, ACETAMINOPHEN 500MG | openfda.generic_name | |
| manufacturer name | Redicare LLC | openfda.manufacturer_name | |
| ndc | package | 71105-011-01 | openfda.package_ndc |
| ndc | package | 71105-011-02 | openfda.package_ndc |
| ndc | product | 71105-011 | openfda.product_ndc |
| ndc11 | package | 71105001101 | derived:openfda.package_ndc |
| ndc11 | package | 71105001102 | derived:openfda.package_ndc |
| rxcui | 198440 | openfda.rxcui | |
| spl id | 2f850cc1-2c48-a305-e063-6294a90a40c7 | id | |
| spl set id | 2f229898-1777-732c-e063-6394a90a76bc | set_id | |
| unii | 362O9ITL9D | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings: Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take ■ more than 4,000mg of acetaminophen in 24 hours ■ with other drugs containing acetaminophen ■ 3 or more alcoholic drinks every day while using this product Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: ■ skin reddening ■ blisters ■ rash If a skin reaction occurs, stop use and seek medical help right away. Do not use ■ with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. ■ if you are allergic to acetaminophen or any of the inactive ingredients in this product Ask a doctor before use if you have liver disease Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin Stop use and ask a doctor if ■ pain gets worse or lasts more than 10 days ■ fever gets worse or lasts more than 3 days ■ new symptoms occur ■ redness or swelling is present. These could be signs of a serious condition If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. Overdose warning: In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
warnings and cautions
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take ■ more than 4,000mg of acetaminophen in 24 hours ■ with other drugs containing acetaminophen ■ 3 or more alcoholic drinks every day while using this product
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include: ■ skin reddening ■ blisters ■ rash If a skin reaction occurs, stop use and seek medical help right away.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.