Lightening Day Cream
- Product NDC
- 51830-019
- 11-digit product format
- 518300019
- Labeler code
- 51830
- Product ID
- 51830-019_944084b6-7eb0-42fd-8f40-5b22812e1001
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DICAPRYLYL CARBONATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- LANGE SAS
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-07-18
- Marketing end
- 0000-00-00
- Substance
- POLYETHYLENE GLYCOL 400
- Active strength
- 3 mg/50mg
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51830-019-04 | Lightening Day Cream | 50 mg in 1 CONTAINER | CREAM | 50 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51830-019 | LIGHTENING DAY CREAM (DICAPRYLYL CARBONATE) CREAM [LANGE SAS] | 2 | Legacy NDC, 1 package rows | 20130213_e62497be-d0ac-4f3e-988f-5d3c2629a08a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 51830-019-04 | 51830001904 | 50 mg in 1 CONTAINER | 50 mg | Historical |