Laser Sunscreen 100
- Product NDC
- 52554-1115
- 11-digit product format
- 525541115
- Labeler code
- 52554
- Product ID
- 52554-1115_63f41ca6-6c48-394c-e053-2991aa0a2b03
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octisalate, Octinoxate, Zinc Oxide, Titanium Dioxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- CMS LAB Inc.
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-16
- Marketing end
- 0000-00-00
- Substance
- OCTISALATE; ZINC OXIDE; TITANIUM DIOXIDE; OCTINOXATE
- Active strength
- 2 g/35mL; g/35mL; g/35mL; g/35mL
- 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 |
|---|
| 52554-1115-1 | Laser Sunscreen 100 | 35 mL in 1 TUBE | CREAM | 35 | | 4 |
| 52554-1115-2 | Laser Sunscreen 100 | 1 in 1 PACKAGE | CREAM | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52554-1115 | LASER SUNSCREEN 100 (OCTISALATE, OCTINOXATE, ZINC OXIDE, TITANIUM DIOXIDE) CREAM [CMS LAB INC.] | 4 | Legacy NDC, 2 package rows | 20180130_62ede81a-ab15-8e88-e053-2991aa0aa069.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52554-1115-1 | 52554111501 | 35 mL in 1 TUBE | 35 ml | | | | | Historical |
| 52554-1115-2 | 52554111502 | 1 TUBE in 1 PACKAGE (52554-1115-2) > 35 mL in 1 TUBE (52554-1115-1) | 1 tube | 2018-01-16 | 0000-00-00 | No | No | Current |