DR HOS PAIN RELIEF MAXIMUM STRENGTH
- Product NDC
- 71447-121
- Requested package NDC
- 71447-121-01
- 11-digit product format
- 714470121
- Labeler code
- 71447
- Product ID
- 71447-121_d382a964-3d0a-9bf6-e053-2a95a90acc39
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor,Menthol
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- LABORATOIRES DRUIDE INC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-03-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-01-11 03:41 UTC · source 2025-01-10 | excluded package | package | 71447-121 | 71447-121-01 | U | Excluded because listing certification expired | excluded / ndc_excluded.zip | 0efc9e666f02… | f202fb6c5f17… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71447-121-01 | 71447012101 | 1 BOX in 1 BOTTLE, SPRAY (71447-121-01) > 118 mL in 1 BOX (71447-121-00) | 1 box | 2021-03-01 | 0000-00-00 | No | No | Current |