Conju Princess BB
- Product NDC
- 59915-1001
- 11-digit product format
- 599151001
- Labeler code
- 59915
- Product ID
- 59915-1001_ebf42107-3f8a-4d91-91be-f346ce1961d0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- arbutin
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Conju Inc
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-01-24
- Marketing end
- 0000-00-00
- Substance
- TITANIUM DIOXIDE; ARBUTIN; ADENOSINE
- Active strength
- 10 mL/100mL; mL/100mL; mL/100mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 59915-1001-1 | Conju Princess BB | 30 mL in 1 TUBE | CREAM | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59915-1001 | CONJU PRINCESS BB (ARBUTIN) CREAM [CONJU INC] | 1 | Legacy NDC, 1 package rows | 20110126_5c6d6598-37a3-4516-9170-fb976e11c1e7.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 59915-1001-1 | 59915100101 | 30 mL in 1 TUBE | 30 ml | Historical |