LUMIOR
- Product NDC
- 60289-296
- 11-digit product format
- 602890296
- Labeler code
- 60289
- Product ID
- 60289-296_14533575-ffe0-4514-b303-a56576d63e86
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Avobenzone, 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; OCTISALATE; OCTOCRYLENE
- Active strength
- 30 mg/mL; mg/mL; mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 60289-296 | LUMIOR MEN FACIAL MOISTURIZER BROAD SPECTRUM SPF 15 (AVOBENZONE, OCTISALATE, AND OCTOCRYLENE) LOTION [AHAVA DEAD SEA LABORATORIES LTD] | 2 | Legacy NDC | 20231116_4c0bdf52-dc2e-43b0-950c-d7ce1f732df8.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60289-296-24 | 60289029624 | 1 BOTTLE, GLASS in 1 CARTON (60289-296-24) > 50 mL in 1 BOTTLE, GLASS | 2020-10-01 | 0000-00-00 | No | No | Current |