Kanjo PAIN RELIEF Gel
- Product NDC
- 35192-039
- 11-digit product format
- 351920039
- Labeler code
- 35192
- Product ID
- 35192-039_ef43bdf4-7e28-0818-e053-2a95a90a466c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- CA-BOTANA INTERNATIONAL
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-31
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 6 g/120g
- 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 | 35192-039 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 35192-039 | 35192-039-02 | D | Discontinued by firm | 2026-10-15 |
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 |
|---|---|---|---|---|---|---|---|---|
| 35192-039-02 | 35192003902 | 120 g in 1 TUBE (35192-039-02) | 120 g | 2020-08-31 | 0000-00-00 | No | No | Current |