Pain Relief Gel
- Product NDC
- 73239-1904
- 11-digit product format
- 732391904
- Labeler code
- 73239
- Product ID
- 73239-1904_95ae7b69-107c-e959-e053-2a95a90a35fe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Camphor, and Menthol gel
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Kanamed Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2019-10-16
- Marketing end
- 0000-00-00
- Substance
- MENTHOL; CAMPHOR (NATURAL)
- Active strength
- 5 mg/100mL; mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73239-1904-1 | Pain Relief Gel | 100 mL in 1 TUBE | GEL | 100 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73239-1904 | PAIN RELIEF GEL (CAMPHOR, AND MENTHOL GEL) GEL [KANAMED INC.] | 1 | Legacy NDC, 1 package rows | 20191025_95ae7b57-3e85-db85-e053-2995a90a741f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 73239-1904-1 | 73239190401 | 100 mL in 1 TUBE | 100 ml | Historical |