BOTANIC TWENTY DAILY SUNBLOCK SPF50
- Product NDC
- 71364-004
- 11-digit product format
- 713640004
- Labeler code
- 71364
- Product ID
- 71364-004_7cb97fc9-59c0-3271-e053-2a91aa0afa5c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- OCTINOXATE, TITANIUM DIOXIDE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- RITZY NOBLE CO., LTD.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-01-01
- Marketing end
- 0000-00-00
- Substance
- OCTINOXATE; TITANIUM DIOXIDE
- Active strength
- 3 g/50mL; g/50mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 71364-004-01 | BOTANIC TWENTY DAILY SUNBLOCK SPF50 | 50 mL in 1 TUBE | LOTION | 50 | | 1 |
| 71364-004-02 | BOTANIC TWENTY DAILY SUNBLOCK SPF50 | 1 in 1 BOX | LOTION | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71364-004 | BOTANIC TWENTY DAILY SUNBLOCK SPF50 (OCTINOXATE, TITANIUM DIOXIDE) LOTION [RITZY NOBLE CO., LTD.] | 1 | Legacy NDC, 2 package rows | 20181212_7cb97fc9-59bf-3271-e053-2a91aa0afa5c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 71364-004-01 | 71364000401 | 50 mL in 1 TUBE | 50 ml | Historical |
| 71364-004-02 | 71364000402 | 1 in 1 BOX | | Historical |