Blue-Emu Pain Relief Micro-Foam
- Product NDC
- 69993-500
- 11-digit product format
- 699930500
- Labeler code
- 69993
- Product ID
- 69993-500_ac8578f6-1d70-496c-a886-c669cc41297f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- TROLAMINE SALICYLATE
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Gregory Pharmaceutical Holdings, Inc. dba NFI Consumer Products
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-04-05
- Marketing end
- 0000-00-00
- Substance
- TROLAMINE SALICYLATE
- Active strength
- 0 g/g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 product | product | 69993-500 | D | Discontinued by firm | 2026-10-02 | ||
| excluded package | package | 69993-500 | 69993-500-35 | D | Discontinued by firm | 2026-10-02 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69993-500-35 | 69993050035 | 99.2 g in 1 CANISTER (69993-500-35) | 99.2 g | 2021-04-05 | 0000-00-00 | No | No | Current |