Appeal Antibac
- Product NDC
- 11084-732
- 11-digit product format
- 110840732
- Labeler code
- 11084
- Product ID
- 11084-732_852d5ed9-b99c-4ac9-910d-3eab1d0ff515
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Triclosan
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Deb USA, Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-07-05
- Marketing end
- 2020-08-01
- Substance
- TRICLOSAN
- Active strength
- 0 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 11084-732 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 11084-732 | 11084-732-27 | D | Discontinued by firm | 2026-08-03 |