Camphotrol
- Product NDC
- 59088-488
- 11-digit product format
- 590880488
- Labeler code
- 59088
- Product ID
- 59088-488_1e2d2f1a-8848-6a76-e063-6394a90ae170
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- camphor, menthol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-01-18
- Substance
- CAMPHOR (SYNTHETIC); MENTHOL
- Active strength
- 4; 10 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Camphotrol
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CAMPHOR (SYNTHETIC) | 4 g/100g |
| MENTHOL | 10 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 5TJD82A1ET, L7T10EIP3A |
| Rxcui | 1039731 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-488-07 | Camphotrol | 85 g in 1 BOTTLE, WITH APPLICATOR | GEL | 85 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-488 | CAMPHOTROL (CAMPHOR, MENTHOL) GEL [PURETEK CORPORATION] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240727_ccac9f37-a374-4765-e053-2a95a90ad2f7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59088-488-07 | 59088048807 | 85 g in 1 BOTTLE, WITH APPLICATOR (59088-488-07) | 85 g | 2022-01-18 | 0000-00-00 | No | No | Current |