SUMMER GELEE SPF-4
NDC 84281-476, HOMOSALATE, OCTISALATE, gel, from SUMMER GELEE LLC.
- Product NDC
- 84281-476
- Status
- Listed
- Labeler
- SUMMER GELEE LLC
- Dosage form
- GEL
- 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/84281-476 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HOMOSALATE20 mg/mL
- OCTISALATE20 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 84281-476-00 | 84281047600 | 92.26 mL in 1 TUBE (84281-476-00) |
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 84281-476 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/84281-476 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 84281-476. 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.