AER Pre-moistened Witch Hazel Pad
NDC 50289-3250, Witch Hazel, solution, from Birchwood Laboratories LLC.
- Product NDC
- 50289-3250
- Status
- Listed
- Labeler
- Birchwood Laboratories LLC
- Dosage form
- SOLUTION
- Route
- RECTAL, TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M015
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50289-3250 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- WITCH HAZEL500 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50289-3250-1 | 50289325001 | 40 APPLICATOR in 1 JAR (50289-3250-1) / 2.8 mL in 1 APPLICATOR |
Linked data
RxNorm, label and prices
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 50289-3250 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50289-3250 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50289-3250. 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.