EB Epicurus SPF 50 The Sunscreen
- Product NDC
- 81901-001
- 11-digit product format
- 819010001
- Labeler code
- 81901
- Product ID
- 81901-001_c3c98d72-67d3-372c-e053-2a95a90a8474
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, OCTOCRYLENE, OCTINOXATE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- BIOCROWN BIOTECHNOLOGY CO., LTD
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-06-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; OCTOCRYLENE; AVOBENZONE
- Active strength
- 30 mg/mL; mg/mL; mg/mL
- 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 |
|---|
| 81901-001-35 | EB Epicurus SPF 50 The Sunscreen | 35 mL in 1 BOTTLE | LOTION | 35 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81901-001 | EB EPICURUS SPF 50 THE SUNSCREEN (AVOBENZONE, OCTOCRYLENE, OCTINOXATE) LOTION [BIOCROWN BIOTECHNOLOGY CO., LTD] | 1 | Legacy NDC, 1 package rows | 20210603_c3c98d72-67d2-372c-e053-2a95a90a8474.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81901-001-35 | 81901000135 | 35 mL in 1 BOTTLE (81901-001-35) | 35 ml | 2021-06-01 | 0000-00-00 | No | No | Current |