NDC 70381-112-01 - Acne Control Clarifying Body Spry
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
- 70381-112
- Requested NDC
- 70381-112-01
- Package NDCs from labels
- 70381-112-01, 70381-112-02
- Manufacturer
- Murad, LLC | Cosway Company, Inc.
- Effective date
- 2021-07-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Acne Control Clarifying Body Spray | Murad, LLC | Cosway Company, Inc. | 2021-07-02 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 70381-112-02 | 2023-01-30 | C162847 | 48780-1 | f386c64a-38f3-0266-e053-dadaa90a7c1a | Acne Control Clarifying Body Spray |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70381-112-01 | Acne Control Clarifying Body Spry | 130 mL in 1 BOTTLE | SPRAY | 130 | 4 | |
| 70381-112-02 | Acne Control Clarifying Body Spry | 1 in 1 CARTON | SPRAY | 1 | 4 |
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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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.