NDC 69153-130-01 - All Nations A D C Special Program
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
- 69153-130
- Requested NDC
- 69153-130-01
- Package NDCs from labels
- 69153-130-01, 69153-130-02
- Manufacturer
- AN Co Ltd.
- Effective date
- 2017-06-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| All Nations A D C Special Program - AN Co Ltd. | AN Co Ltd. | 2017-06-27 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69153-130-02 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-40d7-a910-e053-dadaa90a0b85 | 811f4b63-48cc-44c8-880d-3379f68bd441 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69153-130-01 | All Nations A D C Special Program | 6 mL in 1 CONTAINER | SOLUTION | 6 | 1 | |
| 69153-130-02 | All Nations A D C Special Program | 10 in 1 CARTON | SOLUTION | 10 | 1 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| c3e7e3e2-d5bd-4bd5-a757-18e3c0de1765 | 811f4b63-48cc-44c8-880d-3379f68bd441 | 2017-06-27 | Warnings | c3e7e3e2-d5bd-4bd5-a757-18e3c0de1765 811f4b63-48cc-44c8-880d-3379f68bd441 | ||
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.