NDC 66854-025-04 - SPA SKILHA HELIOPROT AB SPF 40
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
- 66854-025
- Requested NDC
- 66854-025-04
- Package NDCs from labels
- 66854-025-01, 66854-025-02, 66854-025-03, 66854-025-04, 66854-025-05
- Manufacturer
- SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
- Effective date
- 2012-06-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BEMOTRIZINOL - SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS | SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS | 2012-06-07 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 66854-025-01 | SPA SKILHA HELIOPROT AB SPF 40 | 9 g in 1 JAR | CREAM | 9 | 1 | |
| 66854-025-02 | SPA SKILHA HELIOPROT AB SPF 40 | 33 g in 1 JAR | CREAM | 33 | 1 | |
| 66854-025-03 | SPA SKILHA HELIOPROT AB SPF 40 | 60 g in 1 TUBE | CREAM | 60 | 1 | |
| 66854-025-04 | SPA SKILHA HELIOPROT AB SPF 40 | 15 g in 1 TUBE | CREAM | 15 | 1 | |
| 66854-025-05 | SPA SKILHA HELIOPROT AB SPF 40 | 20 in 1 BOX | CREAM | 20 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 66854-025 | SPA SKILHA HELIOPROT AB SPF 40 (BEMOTRIZINOL,OCTINOXATE,AVOBENZONE,TITANIUM DIOXIDE) CREAM [SPAI-SONS PHARMACEUTICAL INTERNATIONAL COSMETICS] | 1 | Legacy NDC, 5 package rows | 20120630_ff3ef5f7-4846-48c6-aebc-26723f7f2320.zip |
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.