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NDC 50390-232, OCTINOXATE, OXYBENZONE, cream, from Amway Corp.
- Product NDC
- 50390-232
- Status
- Listed
- Labeler
- Amway Corp
- Dosage form
- CREAM
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- M020
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50390-232 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OCTINOXATE75 mg/mL
- OXYBENZONE5 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50390-232-00 | 50390023200 | 1 BOTTLE, PLASTIC in 1 CARTON (50390-232-00) / 30 mL in 1 BOTTLE, PLASTIC |
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 50390-232 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50390-232 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50390-232. 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.