KinetiCream Pain Relieving Topical Analgesic
- Product NDC
- 58611-971
- 11-digit product format
- 586110971
- Labeler code
- 58611
- Product ID
- 58611-971_4ecb6ace-0671-e88b-e063-6394a90a379c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Phoenix Bioperformance Products LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-02-02
- Substance
- MENTHOL
- Active strength
- 20 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- KinetiCream Pain Relieving Topical Analgesic
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A |
| Rxcui | 1102253 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 58611-971-00 | KinetiCream Pain Relieving Topical Analgesic | 101 mL in 1 BOTTLE | CREAM | 101 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 58611-971-00 | 58611097100 | 101 mL in 1 BOTTLE (58611-971-00) | 101 ml | 2026-02-02 | No | No | Current |