NDC 68678-053 - BIOEASE PAIN RELIEVING COLD THERAPY
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
- 68678-053
- Package NDCs from labels
- 68678-053-03
- Manufacturer
- AHC Ventures Corp DBA Cryoderm
- Effective date
- 2014-02-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| BIOEASE PAIN RELIEVING COLD THERAPY - AHC Ventures Corp DBA Cryoderm | AHC Ventures Corp DBA Cryoderm | 2014-02-02 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68678-053-03 | 2019-11-27 | C162847 | 48780-1 | 9855e2a2-4cda-60a7-e053-dbdaa90a05bd | BIOEASE® Pain Relieving Cold Therapy Roll-On |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68678-053-03 | BIOEASE PAIN RELIEVING COLD THERAPY | 95 mL in 1 BOTTLE | GEL | 95 | 2 |
DailyMed Dashboard NDC Coverage#
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.