NDC 69231-032-01 - CLE CCC Warm Deep
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
- 69231-032
- Requested NDC
- 69231-032-01
- Package NDCs from labels
- 69231-032-01, 69231-032-02
- Manufacturer
- KW ABSC, INC. | Cit Co., Ltd
- Effective date
- 2024-12-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CLE CCC Warm Deep - KW ABSC, INC. | Cit Co., Ltd | KW ABSC, INC. | Cit Co., Ltd | 2024-12-19 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69231-032-01 | CLE CCC Warm Deep | 30 mL in 1 CONTAINER | CREAM | 30 | 2 | |
| 69231-032-02 | CLE CCC Warm Deep | 1 in 1 PACKAGE | CREAM | 1 | 2 |
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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| SHISEIDO ULTIMATE SUN PROTECTOR | AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE | SHISEIDO AMERICAS CORPORATION | 00ec7d9c-8550-45ce-8d0a-ef2caf84f98d | 2025-03-21 | Warnings | M020 G63QQF2NOX 4X49Y0596W |
| Obagi Skintrinsiq Clarifiying Protocol | SALICYLIC ACID, TITANIUM DIOXIDE, AND ZINC OXIDE | Obagi Cosmeceuticals LLC | 08ba9ea8-73fd-472b-9cc4-67df167352ec | 2025-03-21 | Warnings | M020 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.