NDC 51439-007-01 - Acne Clearning Treatment Face
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
- 51439-007
- Requested NDC
- 51439-007-01
- Package NDCs from labels
- 51439-007-01, 51439-007-02
- Manufacturer
- CarePluss Pharma S.A. de C.V.
- Effective date
- 2013-03-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Acne Clearning Treatment Face - CarePluss Pharma S.A. de C.V. | CarePluss Pharma S.A. de C.V. | 2013-03-20 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51439-007-02 | 2019-11-27 | C162847 | 48780-1 | 9855d018-ea92-cd31-e053-dbdaa90ab51a | 0001eaa9-e890-4e94-9d44-47a0f3086a02 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51439-007-01 | Acne Clearning TreatmentFace | .024 mg in 1 BOTTLE | LIQUID | .024 | 2 | |
| 51439-007-02 | Acne Clearning TreatmentFace | 3 in 1 BOX | LIQUID | 3 | 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.
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| Acne Treatment | BENZOYL PEROXIDE | Walmart Inc. | 950edb4e-fbba-41e3-9ec5-973806e555e7 | 2026-02-27 | Warnings, Adverse reactions | W9WZN9A0GM |
| Body Wash | SALICYLIC ACID | Walmart Inc. | c31a5629-66c3-47a7-96ea-9987b2be82af | 2026-02-27 | Warnings, Adverse reactions | O414PZ4LPZ |
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| Acne Treatment | BENZOYL PEROXIDE | The Kroger Co. | a6526d73-4094-45b7-97f0-561dd10d61e2 | 2026-02-26 | Warnings, Adverse reactions | W9WZN9A0GM |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.