LUMIOR
- Product NDC
- 60289-297
- 11-digit product format
- 602890297
- Labeler code
- 60289
- Product ID
- 60289-297_0da19f10-ba81-4b1a-8393-6ab5d7352d48
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, Homosalate, Octisalate, and Octocrylene
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- AHAVA Dead Sea Laboratories Ltd
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-10-01
- 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
- 2021-12-31
- 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#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60289-297 | LUMIOR DAYLIGHT MOISTURIZER BROAD SPECTRUM SPF 20 (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) LOTION [AHAVA DEAD SEA LABORATORIES LTD] | 2 | Legacy NDC | 20231116_7e76ee98-6483-4d3f-9f5a-c524abf01486.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60289-297-24 | 60289029724 | 1 JAR in 1 CARTON (60289-297-24) > 50 mL in 1 JAR | 1 jar | 2020-10-01 | 0000-00-00 | No | No | Current |