MD Glam SPF 50
- Product NDC
- 68062-9000
- 11-digit product format
- 680629000
- Labeler code
- 68062
- Product ID
- 68062-9000_efd53834-7fb7-818b-e053-2995a90a99d3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- octinoxate
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-12-14
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 4 mg/50mL; mg/50mL
- 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 |
|---|
| 68062-9000 | MD GLAM SPF 50 (OCTINOXATE) LOTION [SPA DE SOLEIL] | 2 | Legacy NDC | 20221217_efd53834-7fb6-818b-e053-2995a90a99d3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68062-9000-1 | 68062900001 | 50 mL in 1 BOTTLE (68062-9000-1) | 50 ml | 2022-12-14 | 0000-00-00 | No | No | Current |