NanoX Pain Relieving
- Product NDC
- 84804-322
- 11-digit product format
- 848040322
- Labeler code
- 84804
- Product ID
- 84804-322_4cc38936-69fa-299f-e063-6294a90a9e69
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL, METHYL SALICYLATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- MG Science Technologies LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-03-11
- Substance
- MENTHOL; METHYL SALICYLATE
- Active strength
- 40; 100 mg/mL; 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
- NanoX Pain Relieving
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MENTHOL | 40 mg/mL |
| METHYL SALICYLATE | 100 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | L7T10EIP3A, LAV5U5022Y |
| Rxcui | 2698214 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84804-322-01 | NanoX Pain Relieving | 100 mL in 1 TUBE | CREAM | 100 | | 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 |
|---|
| 84804-322-01 | 84804032201 | 100 mL in 1 TUBE (84804-322-01) | 100 ml | 2026-03-12 | No | No | Current |