NDC 57718-200-01 - Mizon Bye Bye Pimple
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
- 57718-200
- Requested NDC
- 57718-200-01
- Package NDCs from labels
- 57718-200-01, 57718-200-02
- Manufacturer
- MIZON CO.,LTD. | GGK CO.,LTD.
- Effective date
- 2018-06-08
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Mizon Bye Bye Pimple - MIZON CO.,LTD. | GGK CO.,LTD. | MIZON CO.,LTD. | GGK CO.,LTD. | 2018-06-08 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 57718-200-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-7f18-f424-e053-dadaa90a57ce | 022b5b74-add8-4d01-a098-8274c979b48d |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 57718-200-01 | Mizon Bye Bye Pimple | 3.5 g in 1 PATCH | PATCH | 3.5 | 2 | |
| 57718-200-02 | Mizon Bye Bye Pimple | 24 in 1 POUCH | PATCH | 24 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| DRMITSUI HYDROCOLLOID WOUND | HYDROCOLLOID | YIYANGYUAN LIFE SCIENCES (HONG KONG) CO., LIMITED | 5438682c-6bc5-83f2-e063-6394a90ac348 | 2026-06-14 | Warnings | 05JZI7B19X |
| cea313b4-17fd-41cd-a758-75970ed6a61b | 022b5b74-add8-4d01-a098-8274c979b48d | 2018-06-08 | Warnings | cea313b4-17fd-41cd-a758-75970ed6a61b 022b5b74-add8-4d01-a098-8274c979b48d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.