NDC 50845-0132-2 - ProBlen DNA RNA Rejuvenation
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50845-0132
- Requested NDC
- 50845-0132-2
- Package NDCs from labels
- 50845-0132-1, 50845-0132-2, 50845-0132-3
- Manufacturer
- Liddell Laboratories, Inc.
- Effective date
- 2012-02-06
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ProBLEN DNA RNA Rejuvenation | Liddell Laboratories, Inc. | 2012-02-06 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0132-3 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c48b-f6ea-e053-dbdaa90aa703 | ProBLEN DNA RNA Rejuvenation |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50845-0132-1 | ProBlen DNA RNA Rejuvenation | 30 mL in 1 BOTTLE, SPRAY | SPRAY | 30 | 1 | |
| 50845-0132-2 | ProBlen DNA RNA Rejuvenation | 1 in 1 CARTON | SPRAY | 1 | 1 | |
| 50845-0132-3 | ProBlen DNA RNA Rejuvenation | 1 in 1 CARTON | SPRAY | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50845-0132 | PROBLEN DNA RNA REJUVENATION (ARNICA MONTANA, AVENA SATIVA, DAMIANA, DNA, KOREAN GINSENG, OLEUM ANIMALE, PITUITARY BOVINUM, RNA, THUJA OCCIDENTALIS, TRIBULUS TERRESTRIS,) SPRAY [LIDDELL LABORATORIES, INC.] | 1 | Legacy NDC, 3 package rows | 20120207_d613f415-dbcf-422a-8ebd-0dcca808d82a.zip |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.