Sun Screen
- Product NDC
- 70445-156
- 11-digit product format
- 704450156
- Labeler code
- 70445
- Product ID
- 70445-156_d4c71a45-c07e-5b55-e053-2a95a90a4228
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Oxybenzone, Titanium Dioxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Webb Business Promotions
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-01-01
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; OCTINOXATE; OCTISALATE; OXYBENZONE
- Active strength
- 4 g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70445-156-01 | Sun Screen | 28.34 g in 1 BOTTLE, PLASTIC | LOTION | 28.34 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70445-156 | SUN SCREEN (OCTINOXATE, OCTISALATE, OXYBENZONE, TITANIUM DIOXIDE) LOTION [WEBB BUSINESS PROMOTIONS] | 6 | Legacy NDC, 1 package rows | 20220105_3f2509c7-2d22-6a8f-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70445-156-01 | 70445015601 | 28.34 g in 1 BOTTLE, PLASTIC (70445-156-01) | 28.34 g | 2009-09-11 | 0000-00-00 | No | No | Current |