Sunscreen
- Product NDC
- 0869-0059
- 11-digit product format
- 008690059
- Labeler code
- 0869
- Product ID
- 0869-0059_9a336b5e-5a7a-46a1-aa70-bbe5f3672505
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-08-17
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 30 mg/mL; mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0869-0059-30 | 00869005930 | 177 mL in 1 TUBE (0869-0059-30) | 177 ml | 2022-08-17 | 0000-00-00 | No | No | Current |