Sulfur Spot Treatment
NDC 70707-440, SULFUR, gel, from Face Reality, Inc.
- Product NDC
- 70707-440
- Status
- Listed
- Labeler
- Face Reality, Inc
- Dosage form
- GEL
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M006
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70707-440 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFUR60 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70707-440-04 | 70707044004 | 118 mL in 1 BOTTLE (70707-440-04) |
| 70707-440-15 | 70707044015 | 1 TUBE in 1 BOX (70707-440-15) / 44 mL in 1 TUBE |
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 70707-440 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70707-440 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70707-440. 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.