outdoor explorer set
- Product NDC
- 59062-5300
- 11-digit product format
- 590625300
- Labeler code
- 59062
- Product ID
- 59062-5300_132c4b8e-b4f3-478d-b6eb-f4496726f568
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Titanium Dioxide, Octisalate, and Zinc Oxide
- Dosage form
- KIT
- Labeler
- KAS Direct LLC dba BabyGanics
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59062-1000-2 | outdoor explorer set | 59 mL in 1 TUBE | LOTION | 59 mL | 50 mg in 1mL | 2 |
| 59062-5300-1 | outdoor explorer set | 1 in 1 PACKAGE | KIT | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59062-5300 | OUTDOOR EXPLORER SET (TITANIUM DIOXIDE, OCTISALATE, AND ZINC OXIDE) KIT [KAS DIRECT LLC DBA BABYGANICS] | 2 | Legacy NDC, 2 package rows | 20210720_726096c2-514a-439a-9697-346ca684c493.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59062-1000-2 | 59062100002 | 59 mL in 1 TUBE | 59 ml | | | | | Historical |
| 59062-5300-1 | 59062530001 | 1 KIT in 1 PACKAGE (59062-5300-1) * 59 mL in 1 TUBE (59062-1000-2) * 177 mL in 1 BOTTLE, SPRAY | 1 kit | 2018-01-01 | 0000-00-00 | No | No | Current |