Dr Young 2p Brightening UV Sun Block SPF50 PA
- Product NDC
- 43948-5003
- 11-digit product format
- 439485003
- Labeler code
- 43948
- Product ID
- 43948-5003_0a5ab7a7-8dff-4daf-a586-0689e0b29f6c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ARBUTIN, ETHYLHEXYL METHOXYCINNAMATE
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- The Doctor's Cosmetic Inc
- Application
- part352
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-11-01
- Marketing end
- 0000-00-00
- Substance
- ARBUTIN; OCTINOXATE
- Active strength
- 1 mL/50mL; mL/50mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 43948-5003-1 | Dr Young 2p Brightening UV Sun Block SPF50 PA | 50 mL in 1 TUBE | CREAM | 50 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43948-5003 | DR YOUNG 2P BRIGHTENING UV SUN BLOCK SPF50 PA (ARBUTIN, ETHYLHEXYL METHOXYCINNAMATE) CREAM [THE DOCTOR'S COSMETIC INC] | 1 | Legacy NDC, 1 package rows | 20091220_d5915e8d-69ee-486a-9fc9-e35562bf967f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 43948-5003-1 | 43948500301 | 50 mL in 1 TUBE | 50 ml | Historical |