Neuracin Topical Gel
NDC 70512-104, Neuracin Topical Analgesic Gel, gel, from SOLA Pharmaceuticals.
- Product NDC
- 70512-104
- Status
- Listed
- Labeler
- SOLA Pharmaceuticals
- Dosage form
- GEL
- 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/70512-104 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- METHYL SALICYLATE300 mg/g
- CAMPHOR (SYNTHETIC)40 mg/g
- MENTHOL, UNSPECIFIED FORM100 mg/g
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70512-104-60 | 70512010460 | 1 TUBE in 1 CARTON (70512-104-60) / 56.7 g in 1 TUBE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 70512-104 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70512-104 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70512-104. 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.