NDC 64479-150 - OzHealth Advanced Arthritis
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
- 64479-150
- Package NDCs from labels
- 64479-150-14, 64479-150-15
- Manufacturer
- SmartScience Laboratories, Inc.
- Effective date
- 2018-06-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OzHealth ADVANCED ARTHRITIS Pain Relief Cream | SmartScience Laboratories, Inc. | 2018-06-13 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 64479-150-14 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-25e1-f424-e053-dadaa90a57ce | OzHealth ADVANCED ARTHRITIS Pain Relief Cream |
| 64479-150-15 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-25e1-f424-e053-dadaa90a57ce | OzHealth ADVANCED ARTHRITIS Pain Relief Cream |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 64479-150-14 | OzHealth Advanced Arthritis | 114 g in 1 JAR | CREAM | 114 | 1 | |
| 64479-150-15 | OzHealth Advanced Arthritis | 114 g in 1 TUBE | CREAM | 114 | 1 | |
| 64479-150-15 | OzHealth Advanced Arthritis | 1 in 1 CARTON | CREAM | 1 | 1 |
DailyMed Dashboard NDC Coverage#
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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| Gas Relief Simethicone 180mg Softgel | SIMETHICONE | NUVICARE LLC | 51484644-eb45-4282-91c6-289169bcbaf6 | 2025-12-19 | Warnings | 92RU3N3Y1O |
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| Tiger Balm White Regular Strength | CAMPHOR (SYNTHETIC) AND MENTHOL | Haw Par Healthcare Ltd. | f406161e-a9c4-47d1-8b21-93b1b7938063 | 2025-12-17 | Warnings | 5TJD82A1ET |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.