ABALONE CRYSTALDOUBLE EX AMPOULE
- Product NDC
- 60611-0006
- 11-digit product format
- 606110006
- Labeler code
- 60611
- Product ID
- 60611-0006_4a58190e-39d8-38bb-e054-00144ff8d46c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Arbutin, Adenosine
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- C&BCOSMETIC Co.,Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2017-03-10
- Marketing end
- 0000-00-00
- Substance
- ARBUTIN; ADENOSINE
- Active strength
- 2 g/100mL; g/100mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 60611-0006-1 | ABALONE CRYSTALDOUBLE EX AMPOULE | 14 in 1 PACKAGE | LIQUID | 14 | | 1 |
| 60611-0006-1 | ABALONE CRYSTALDOUBLE EX AMPOULE | 0.8 mL in 1 SYRINGE | LIQUID | 0.8 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60611-0006 | ABALONE CRYSTALDOUBLE EX AMPOULE (ARBUTIN, ADENOSINE) LIQUID [C&BCOSMETIC CO.,LTD.] | 1 | Legacy NDC, 2 package rows | 20170310_4a58190e-39d7-38bb-e054-00144ff8d46c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 60611-0006-1 | 60611000601 | 14 in 1 PACKAGE | Historical |