Legend Age Whitening Sunscreen
- Product NDC
- 82142-001
- 11-digit product format
- 821420001
- Labeler code
- 82142
- Product ID
- 82142-001_c56ba9d9-f1b6-32b1-e053-2a95a90ad87f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sunscreen
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Guangzhou Fu Zhuang Biotechnology Co.,Ltd.
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-06-23
- Marketing end
- 0000-00-00
- Substance
- HOMOSALATE; OCTOCRYLENE; AVOBENZONE; OCTISALATE
- Active strength
- 10 g/100g; g/100g; g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 82142-001-01 | Legend Age Whitening Sunscreen | 40 g in 1 TUBE | CREAM | 40 | | 1 |
| 82142-001-02 | Legend Age Whitening Sunscreen | 1 in 1 BOX | CREAM | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82142-001 | LEGEND AGE WHITENING SUNSCREEN (SUNSCREEN) CREAM [GUANGZHOU FU ZHUANG BIOTECHNOLOGY CO.,LTD.] | 1 | Legacy NDC, 2 package rows | 20211119_c56ba9d9-f1b5-32b1-e053-2a95a90ad87f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82142-001-01 | 82142000101 | 40 g in 1 TUBE | 40 g | | | | | Historical |
| 82142-001-02 | 82142000102 | 1 TUBE in 1 BOX (82142-001-02) > 40 g in 1 TUBE (82142-001-01) | 1 tube | 2021-11-18 | 0000-00-00 | No | No | Current |