SULISRx Sunburn Relief Kit
- Product NDC
- 87735-003
- 11-digit product format
- 877350003
- Labeler code
- 87735
- Product ID
- 87735-003_5bd70084-eba8-42c4-e063-6294a90afb34
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunburn Relief Kit
- Dosage form
- KIT
- Labeler
- Sephoris Pharmaceuticals, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-09-03
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- SULISRx Sunburn Relief Kit
- Listing expiration
- 2027-12-31
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 87735-003-01 | 87735000301 | 1 KIT in 1 KIT (87735-003-01) * 59 mL in 1 BOTTLE, SPRAY (87735-001-01) * 1 TABLET, FILM COATED in 1 BOTTLE (87735-002-01) | 1 kit | 2026-09-03 | No | No | Current |