NDC 0404-0712-99 - Henry Schein Aspirin
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 0404-0712
- Requested NDC
- 0404-0712-99
- Package NDCs from labels
- 0404-0712-99, 0404-0712-13
- Manufacturer
- Henry Schein, Inc.
- Effective date
- 2021-07-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Henry Schein Aspirin | Henry Schein, Inc. | 2021-07-09 | HUMAN OTC DRUG LABEL |
| Aspirin - Sina Health Inc | Sina Health Inc | 2019-02-04 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| ASPIRIN | ACTIVE INGREDIENT | R16CO5Y76E | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| ASPIRIN | ACTIVE MOIETY | R16CO5Y76E | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| CROSCARMELLOSE SODIUM | INACTIVE INGREDIENT | M28OL1HH48 | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| HYPROMELLOSES | INACTIVE INGREDIENT | 3NXW29V3WO | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| MINERAL OIL | INACTIVE INGREDIENT | T5L8T28FGP | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | HENRY SCHEIN ASPIRIN (ASPIRIN) TABLET, FILM COATED [HENRY SCHEIN, INC.] | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.