NDC 69231-035-01 - CLE CCC Olive Medium 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
- 69231-035
- Requested NDC
- 69231-035-01
- Package NDCs from labels
- 69231-035-01, 69231-035-02
- 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 Olive Medium 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 |
|---|---|---|---|---|---|---|
| 69231-035-01 | CLE CCC Olive Medium Deep | 30 mL in 1 CONTAINER | CREAM | 30 | 2 | |
| 69231-035-02 | CLE CCC Olive Medium 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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| Smart Care Hand Sanitizer Watermelon Wave | ALCOHOL | Shenzhen Lantern Scicence Co.,Ltd. | 4f031f62-e56c-9063-e063-6394a90af9c1 | 2026-04-09 | Warnings | 3K9958V90M |
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| Arizona Sun Sunscreen SPF 8 | SUNSCREEN | Arizona Sun Products | 11e8b612-29be-47ed-e063-6394a90ab9e7 | 2026-04-09 | Warnings | M020 4X49Y0596W 4Y5P7MUD51 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.