PURLISSE BLUE LOTUS DAILY MOISTURIZER
- Product NDC
- 72407-401
- 11-digit product format
- 724070401
- Labeler code
- 72407
- Product ID
- 72407-401_d5d21fcf-0ef2-b187-e053-2a95a90a3abb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Pur-Lisse Beauty, LLC
- Application
- part352
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-04-15
- Marketing end
- 0000-00-00
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE
- Active strength
- 2 g/100mL; g/100mL; g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 72407-401-11 | PURLISSE BLUE LOTUS DAILY MOISTURIZERSPF 30 | 50 mL in 1 BOTTLE | LOTION | 50 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72407-401 | PURLISSE BLUE LOTUS DAILY MOISTURIZER SPF 30 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [PUR-LISSE BEAUTY, LLC] | 4 | Legacy NDC, 1 package rows | 20220118_1c8ec9c9-7984-47dd-8972-d728fdec9af5.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72407-401-11 | 72407040111 | 50 mL in 1 BOTTLE (72407-401-11) | 50 ml | 2020-04-15 | 0000-00-00 | No | No | Current |