NDC 69000-019-01 - Lace Future Resist Broad Spectrum SPF 20 Foundation Delilah
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 69000-019
- Requested NDC
- 69000-019-01
- Package NDCs from labels
- 69000-019-01, 69000-019-02
- Manufacturer
- Delilah Cosmetics | Gotha Cosmetics SRL
- Effective date
- 2014-12-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Titanium Dioxide - Delilah Cosmetics | Gotha Cosmetics SRL | Delilah Cosmetics | Gotha Cosmetics SRL | 2014-12-24 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69000-019-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-be1b-f424-e053-dadaa90a57ce | Lace Future Resist Broad Spectrum SPF 20 Foundation |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69000-019-01 | Lace Future Resist Broad Spectrum SPF 20 FoundationDelilah | 38 mL in 1 PACKAGE | LOTION | 38 | 6 | |
| 69000-019-02 | Lace Future Resist Broad Spectrum SPF 20 FoundationDelilah | 1 in 1 CARTON | LOTION | 1 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.