Avobenzone, Homosalate, Octisalate, Octocrylene
- Product NDC
- 0869-0769
- 11-digit product format
- 008690769
- Labeler code
- 0869
- Product ID
- 0869-0769_f116b709-221d-45f7-bd70-8a37abb694e9
- 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
- 2016-01-12
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE
- Active strength
- 30 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 |
|---|
| 0869-0769 | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE LOTION [VI-JON, LLC] | 15 | Legacy NDC | 20250507_791e308f-c6ff-4763-9554-5e8863bfffcb.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0869-0769-34 | 00869076934 | 236 mL in 1 BOTTLE, PLASTIC (0869-0769-34) | 236 ml | 2016-01-12 | 0000-00-00 | No | No | Current |