NDC 69231-034-01 - CLE CCC Golden Medium
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
- 69231-034
- Requested NDC
- 69231-034-01
- Package NDCs from labels
- 69231-034-01, 69231-034-02
- 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 Golden Medium - 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 |
|---|---|---|---|---|---|---|
| 69231-034-01 | CLE CCC Golden Medium | 30 mL in 1 CONTAINER | CREAM | 30 | 2 | |
| 69231-034-02 | CLE CCC Golden Medium | 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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| LAVENDER SCENTED HAND SANITIZER | ALCOHOL | FOURSTAR GROUP USA, INC. | 0e5e21c3-9ee5-44be-988a-f82ac9523059 | 2025-02-25 | Warnings | 3K9958V90M |
| ALOE SCENTED HAND SANITIZER | ALCOHOL | FOURSTAR GROUP USA, INC. | aacde143-ecf1-47ce-ada3-8e74551d0659 | 2025-02-25 | Warnings | 3K9958V90M |
| EUCALYPTUS SCENTED HAND SANITIZER | ALCOHOL | FOURSTAR GROUP USA, INC. | 068ed8c0-1fff-42dd-a217-684201c16023 | 2025-02-25 | Warnings | 3K9958V90M |
| SHEA BUTTER SCENTED HAND SANITIZER | ALCOHOL | FOURSTAR GROUP USA, INC. | 669451fa-7557-4ef5-a668-fe4fea1f0c9b | 2025-02-25 | Warnings | 3K9958V90M |
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| Rida Hair Research Institute | AVOBENZONE,OCTISALATE,OCTOCRYLENE | Rida LLC | ece9dfd8-5f40-49b4-a97e-d4e6ffdb1dca | 2025-02-25 | Warnings | M020 4X49Y0596W |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.