Sunscreen 100
- Product NDC
- 52554-1111
- 11-digit product format
- 525541111
- Labeler code
- 52554
- Product ID
- 52554-1111_5bec4efd-2512-e6e1-e053-2a91aa0af4df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- CMS LAB Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-10-19
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE
- Active strength
- 1 g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 52554-1111-1 | Sunscreen 100 | 50 mL in 1 TUBE | CREAM | 50 | | 3 |
| 52554-1111-2 | Sunscreen 100 | 1 in 1 PACKAGE | CREAM | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52554-1111 | SUNSCREEN 100 (TITANIUM DIOXIDE) CREAM [CMS LAB INC.] | 3 | Legacy NDC, 2 package rows | 20171105_5bec4efd-2511-e6e1-e053-2a91aa0af4df.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 52554-1111-1 | 52554111101 | 50 mL in 1 TUBE | 50 ml | Historical |
| 52554-1111-2 | 52554111102 | 1 in 1 PACKAGE | | Historical |