Sunlight Daily Facial
- Product NDC
- 76150-293
- 11-digit product format
- 761500293
- Labeler code
- 76150
- Product ID
- 76150-293_bff108d1-de70-6d4a-e053-2995a90a6937
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Bell International Laboratories, Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-04-14
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 13 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76150-293-34 | 76150029334 | 30 mL in 1 BOTTLE, GLASS (76150-293-34) | 30 ml | 2021-04-14 | 0000-00-00 | No | No | Current |