Luminosity Activation Day Edition
- Product NDC
- 83108-100
- 11-digit product format
- 831080100
- Labeler code
- 83108
- Product ID
- 83108-100_450e0206-d7d4-bd87-e063-6394a90a3c3e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ZINC OXIDE
- Dosage form
- KIT
- Labeler
- Rationale Group Pty Ltd
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-11-15
- Marketing end
- 2026-09-01
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Luminosity Activation Day Edition
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 83108-100-00 | Luminosity Activation Day Edition | 1 in 1 KIT | KIT | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83108-100 | LUMINOSITY ACTIVATION DAY EDITION (ZINC OXIDE) KIT [RATIONALE GROUP PTY LTD] | 1 | Current NDC, 1 package rows | 20231115_ba026282-38a6-4dd3-aa5a-fb6d215accc1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 83108-100-00 | 83108010000 | 1 KIT in 1 KIT (83108-100-00) * 3 mL in 1 BOTTLE (83108-001-13) | 1 kit | 2023-11-15 | 2026-09-01 | No | No | Historical |