AFCO 5508 Sanifect Foam-E II
NDC 66949-139, Ethanol, liquid, from Zep Inc..
- Product NDC
- 66949-139
- Status
- Listed
- Labeler
- Zep Inc.
- Dosage form
- LIQUID
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- 505G(a)(3)
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/66949-139 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CHLOROXYLENOL2081980 mg/208198mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 66949-139-01 | 66949013901 | 208198 mL in 1 DRUM (66949-139-01) |
| 66949-139-02 | 66949013902 | 6000 mL in 1 CASE (66949-139-02) |
| 66949-139-03 | 66949013903 | 3785 mL in 1 CASE (66949-139-03) |
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 66949-139 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/66949-139 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 66949-139. 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.