NDC 72220-002-01 - MDP PEPTIDE 9 BIO SUN PRO
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
- 72220-002
- Requested NDC
- 72220-002-01
- Package NDCs from labels
- 72220-002-01, 72220-002-02, 72220-002-03, 72220-002-04
- Manufacturer
- SKINIDEA CO., LTD | Cosmax, Inc.
- Effective date
- 2026-07-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| MDP PEPTIDE 9 BIO SUN PRO - SKINIDEA CO., LTD | Cosmax, Inc. | SKINIDEA CO., LTD | Cosmax, Inc. | 2026-07-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72220-002-01 | MDP PEPTIDE 9 BIO SUN PRO | 20 g in 1 CONTAINER | STICK | 20 | 3 | |
| 72220-002-02 | MDP PEPTIDE 9 BIO SUN PRO | 1 in 1 CARTON | STICK | 1 | 3 | |
| 72220-002-03 | MDP PEPTIDE 9 BIO SUN PRO | 20 g in 1 CONTAINER | STICK | 20 | 3 | |
| 72220-002-04 | MDP PEPTIDE 9 BIO SUN PRO | 1 in 1 CARTON | STICK | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 72220-002 | MDP PEPTIDE 9 BIO SUN PRO (HOMOSALATE, OCTOCRYLENE, ETHYLHEXYL SALICYLATE, BUTYL METHOXYDIBENZOYLMETHANE) STICK [SKINIDEA CO., LTD] | 1 | Current NDC, 4 package rows | 20241116_26db53cd-dd82-8790-e063-6394a90a92b1.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.