Ultra UV Defense SPF 30
- Product NDC
- 58469-6100
- 11-digit product format
- 584696100
- Labeler code
- 58469
- Product ID
- 58469-6100_244b582b-350a-382e-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Jenelt Cosmetics
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2014-03-26
- Marketing end
- 0000-00-00
- Substance
- ZINC OXIDE
- Active strength
- 0 mg/g
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 58469-6100-1 | Ultra UV Defense SPF 30 | 60 g in 1 TUBE | CREAM | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 58469-6100 | ULTRA UV DEFENSE SPF 30 (ZINC OXIDE) CREAM [JENELT COSMETICS] | 1 | Legacy NDC, 1 package rows | 20151112_244b582b-3509-382e-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 58469-6100-1 | 58469610001 | 60 g in 1 TUBE | 60 g | Historical |