Phoenix KinetiCream Anti-inflammatory and Pain Relief
- Product NDC
- 58611-032
- 11-digit product format
- 586110032
- Labeler code
- 58611
- Product ID
- 58611-032_b69ae790-4600-38e5-e053-2a95a90aad02
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Phoenix Bioperformance Products, LLC
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2013-05-22
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58611-032-04 | 58611003204 | 118 mL in 1 TUBE (58611-032-04) | 118 ml | 2017-02-22 | 0000-00-00 | No | No | Current |