BENOVA PAIN AND ITCH RELIEF
- Product NDC
- 87150-001
- 11-digit product format
- 871500001
- Labeler code
- 87150
- Product ID
- 87150-001_42513ee2-8b41-a9f3-e063-6394a90a9386
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, 0.11%
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- BENOVA RX LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-15
- Substance
- MENTHOL
- Active strength
- 1.1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87150-001-03 | 87150000103 | 90 mL in 1 BOTTLE, WITH APPLICATOR (87150-001-03) | 90 ml | 2025-12-15 | No | No | Historical |