North Woods Derma Gel Clear
NDC 53125-801, Alcohol, gel, from Superior Chemical Corporation.
- Product NDC
- 53125-801
- Status
- Listed
- Labeler
- Superior Chemical Corporation
- Dosage form
- GEL
- 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/53125-801 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALCOHOL.7 mL/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 53125-801-04 | 53125080104 | 3780 mL in 1 BOTTLE, PLASTIC (53125-801-04) |
| 53125-801-29 | 53125080129 | 1000 mL in 1 BAG (53125-801-29) |
| 53125-801-57 | 53125080157 | 550 mL in 1 BOTTLE, PUMP (53125-801-57) |
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 53125-801 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/53125-801 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 53125-801. 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.