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NDC 49967-895, Sulfur, lotion, from L'Oreal USA Products Inc.
- Product NDC
- 49967-895
- Status
- Listed
- Labeler
- L'Oreal USA Products Inc
- Dosage form
- LOTION
- 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/49967-895 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFUR100 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 49967-895-01 | 49967089501 | 1 TUBE in 1 CARTON (49967-895-01) / 20 mL in 1 TUBE |
| 49967-895-02 | 49967089502 | 3 mL in 1 PACKET (49967-895-02) |
| 49967-895-03 | 49967089503 | 1.5 mL in 1 PACKET (49967-895-03) |
| 49967-895-04 | 49967089504 | 3 mL in 1 TUBE (49967-895-04) |
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 49967-895 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/49967-895 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 49967-895. 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.