Biofreeze Professional
NDC 59316-835, MENTHOL, spray, from Reckitt Benckiser LLC.
- Product NDC
- 59316-835
- Status
- Listed
- Labeler
- Reckitt Benckiser LLC
- Dosage form
- SPRAY
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M017
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59316-835 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- MENTHOL130 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 59316-835-20 | 59316083520 | 118 mL in 1 BOTTLE (59316-835-20) |
| 59316-835-22 | 59316083522 | 2 BOTTLE in 1 CARTON (59316-835-22) / 118 mL in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
RxNorm links no concept to this product's packages.
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 59316-835 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59316-835 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59316-835. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.