LUMIOR
- Product NDC
- 60289-295
- 11-digit product format
- 602890295
- Labeler code
- 60289
- Product ID
- 60289-295_734affa3-5a92-41ac-87a7-3da18af4aad8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- avobenzone, homosalate, and octisalate
- Dosage form
- CREAM
- 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
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60289-295 | LUMIOR EXCLUSIVE DAY BROAD SPECTRUM SPF 20 (AVOBENZONE, HOMOSALATE, AND OCTISALATE) CREAM [AHAVA DEAD SEA LABORATORIES LTD] | 3 | Legacy NDC | 20231109_c55d2eb3-d695-4309-b9b4-6725483d8af4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60289-295-24 | 60289029524 | 1 JAR in 1 CARTON (60289-295-24) > 50 mL in 1 JAR | 1 jar | 2020-10-01 | 0000-00-00 | No | No | Current |