Sunscreen
- Product NDC
- 0869-0940
- 11-digit product format
- 008690940
- Labeler code
- 0869
- Product ID
- 0869-0940_c4ebda60-d0d6-464d-b55d-43713bd96854
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Vi-Jon, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-07-22
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0869-0940 | SUNSCREEN (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [VI-JON, LLC] | 5 | Legacy NDC | 20240402_e7019341-8d8f-4755-88d7-b2a9d9011362.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0869-0940-34 | 00869094034 | 236 mL in 1 BOTTLE (0869-0940-34) | 236 ml | 2022-07-22 | 0000-00-00 | No | No | Current |