Powerproof Sunscreen 100
- Product NDC
- 52554-1112
- 11-digit product format
- 525541112
- Labeler code
- 52554
- Product ID
- 52554-1112_d7a17996-5508-41a4-9067-1dfe1b564551
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Octinoxate, Zinc Oxide, Titanium Dioxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- CMS LAB Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-11-01
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTINOXATE; ZINC OXIDE; TITANIUM DIOXIDE
- Active strength
- 3 g/50mL; 1/50mL; g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 52554-1112-1 | Powerproof Sunscreen 100 | 50 mL in 1 TUBE | CREAM | 50 | | 3 |
| 52554-1112-2 | Powerproof 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 |
|---|
| 52554-1112 | POWERPROOF SUNSCREEN 100 (HOMOSALATE, OCTINOXATE, ZINC OXIDE, TITANIUM DIOXIDE) CREAM [CMS LAB INC.] | 3 | Legacy NDC, 2 package rows | 20171107_e9a80816-2f04-45be-96aa-9be2e5e9d2f9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52554-1112-1 | 52554111201 | 50 mL in 1 TUBE | 50 ml | | | | | Historical |
| 52554-1112-2 | 52554111202 | 1 TUBE in 1 PACKAGE (52554-1112-2) > 50 mL in 1 TUBE (52554-1112-1) | 1 tube | 2017-11-01 | 0000-00-00 | No | No | Current |