rootree Mobitherapy UV Sun Shield
- Product NDC
- 72441-070
- 11-digit product format
- 724410070
- Labeler code
- 72441
- Product ID
- 72441-070_112bf256-6d27-4ea6-a94d-bf49ad9353b1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Octinoxate, Octisalate, Titanium Dioxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- KTCS Corporation
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-07-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE
- Active strength
- 4 g/60g; g/60g; g/60g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 72441-070-01 | rootree Mobitherapy UV Sun Shield | 60 g in 1 CONTAINER | CREAM | 60 | | 2 |
| 72441-070-02 | rootree Mobitherapy UV Sun Shield | 1 in 1 CARTON | CREAM | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72441-070 | ROOTREE MOBITHERAPY UV SUN SHIELD (OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE) CREAM [KTCS CORPORATION] | 2 | Legacy NDC, 2 package rows | 20201231_c02c9385-21b8-4d80-bbdc-e1587aca2a51.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72441-070-01 | 72441007001 | 60 g in 1 CONTAINER | 60 g | | | | | Historical |
| 72441-070-02 | 72441007002 | 1 CONTAINER in 1 CARTON (72441-070-02) > 60 g in 1 CONTAINER (72441-070-01) | 1 container | 2018-07-01 | 0000-00-00 | No | No | Current |