Ultra Sunscreen
NDC 85448-003, Octinoxate, Octisalate, Titanium Dioxide, emulsion, from Jiangsu Senwo Medical Technology Co., Ltd..
- Product NDC
- 85448-003
- Status
- Listed
- Labeler
- Jiangsu Senwo Medical Technology Co., Ltd.
- Dosage form
- EMULSION
- 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/85448-003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- OCTINOXATE.09 g/mL
- OCTISALATE.035 g/mL
- TITANIUM DIOXIDE.027 g/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 85448-003-01 | 85448000301 | 473 mL in 1 BOTTLE (85448-003-01) |
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 85448-003 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/85448-003 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 85448-003. 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.