NDC11 87236000701
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 87236-0007-01 | 87236-0007 |
| 87236-0007-1 | 87236-0007 |
| 87236-007-01 | 87236-007 |
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 87236-007 | 87236-007-01 | D | Discontinued by firm | 2026-08-03 |
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 |
|---|---|---|---|---|---|---|
| Zinc Oxide Skin Protectant | ZINC OXIDE 20% | Aldermed Inc. | a55ac5b4-bac7-4d2a-8ac8-c3eaf7e89e52 | 2026-05-04 | Warnings | 87236-007-01 87236-007 87236000701 |