NDC 69231-014-01 - CLE Essence Air Cushion Medium Light
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
- 69231-014
- Requested NDC
- 69231-014-01
- Package NDCs from labels
- 69231-014-01, 69231-014-02
- Manufacturer
- KW ABSC, INC. | Cit Co., Ltd.
- Effective date
- 2018-08-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| 69231-014_CLE Essence Air Cushion Medium Light | KW ABSC, INC. | Cit Co., Ltd. | 2018-08-15 | HUMAN OTC DRUG LABEL |
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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| skin MD | OCTINOXATE, OCTISALATE, HOMOSALATE | 21st Century Formulations | e809e1d3-0a6d-730d-e053-2a95a90aedb9 | 2025-11-13 | Warnings | 4X49Y0596W 4Y5P7MUD51 |
| BLISTER HP | JUGLANS CINEREA BRANCH BARK/ROOT BARK, POTASSIUM IODIDE, LYCOPODIUM CLAVATUM SPORE, MERCURY, SODIUM CHLORIDE, NITRIC ACID, PHOSPHORUS, RANUNCULUS BULBOSUS, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, THUJA OCCIDENTALIS LEAFY TWIG. | Natural Creations, Inc. | e76f05e7-6d7b-4d2e-ba26-bf776bf0e657 | 2025-11-13 | Warnings | 451W47IQ8X |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.