NDC11 00116102185
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 |
|---|---|
| 00116-1021-85 | 00116-1021 |
| 0116-1021-85 | 0116-1021 |
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 | 0116-1021 | 0116-1021-85 | D | Discontinued by firm | 2026-08-17 |
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 |
|---|---|---|---|---|---|---|
| DYNA-HEX 2 | CHLORHEXIDINE GLUCONATE | Xttrium Laboratories, Inc. | 6cc89ac1-baef-40bb-85a3-d9ae9e3e7a63 | 2026-04-27 | Warnings | 0116-1021-85 0116-1021 00116102185 |
| DYNA-HEX 2 | CHLORHEXIDINE GLUCONATE | Xttrium Laboratories, Inc. | 6e5f9616-ddf5-19c4-e053-2991aa0a372a | 2025-04-30 | Warnings | 0116-1021 |