NDC 62041-320-01 - AAPE Skin Ampoule
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
- 62041-320
- Requested NDC
- 62041-320-01
- Package NDCs from labels
- 62041-320-01, 62041-320-02
- Manufacturer
- PROSTEMICS Co., Ltd. | Prostemics Co., Ltd. Factory
- Effective date
- 2021-05-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AAPE Skin Ampoule - PROSTEMICS Co., Ltd. | Prostemics Co., Ltd. Factory | PROSTEMICS Co., Ltd. | Prostemics Co., Ltd. Factory | 2021-05-28 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 62041-320-02 | 2024-01-30 | C162847 | 48780-1 | 1030e365-6521-111a-e063-dadaa90a10e2 | 65c077dc-ef02-43db-8ce7-14cfa1d27ae9 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62041-320-01 | AAPE Skin Ampoule | 6 mL in 1 CONTAINER | LIQUID | 6 | 1 | |
| 62041-320-02 | AAPE Skin Ampoule | 6 in 1 CARTON | LIQUID | 6 | 1 |
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 |
|---|---|---|---|---|---|---|
| STERILE WATER | STERILE WATER | HF Acquisition Co. LLC, DBA HealthFirst | 74ed2a6f-824c-a1ff-e053-2a91aa0a57c0 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 77bd3c0f-f4ab-7cfa-e053-2a91aa0a1b83 | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 7610bf80-61b7-982f-e053-2a91aa0ac1bb | 2025-01-09 | Warnings, Adverse reactions | 059QF0KO0R |
| T-27 | WATER | DNA Labs, Inc. | f0e9afd7-64a4-4b85-9c5f-4bf07ba4b481 | 2025-01-09 | Warnings | 059QF0KO0R |
| Sterile Water | STERILE WATER FOR INJECTION | Medefil, Inc. | 99e99a50-82d5-aff6-e053-2a95a90a8c56 | 2025-01-08 | Warnings, Adverse reactions | 059QF0KO0R |
| BACTERIOSTATIC WATER | BACTERIOSTATIC WATER | HF Acquisition Co LLC, DBA HealthFirst | 99b0ef9b-600a-40dc-e053-2a95a90aa07e | 2025-01-08 | Warnings, Adverse reactions | 059QF0KO0R |
| STERILE WATER | STERILE WATER | HF Acquisition Co LLC, DBA HealthFirst | 99b1cb12-0b2d-0c0f-e053-2a95a90ac3b6 | 2025-01-08 | Warnings, Adverse reactions | 059QF0KO0R |
| TURMERICFaceCream | NIACINAMIDE | Shengnan (Guangzhou) Cosmetics Co., LTD | 2b0652be-a216-d66b-e063-6394a90a0b28 | 2025-01-06 | Warnings | 25X51I8RD4 |
| Milia Remover Treatment | MILIA REMOVER | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 0a8c7bdb-19f4-54c9-e063-6394a90ac5f5 | 2025-01-04 | Warnings | 25X51I8RD4 |
| Dr.Jucre Rebirth BB | TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE, NIACINAMIDE, ADENOSINE | NATURECELL CO., LTD. | 2ab403df-29b3-75af-e063-6394a90a6ca4 | 2025-01-02 | Warnings | 25X51I8RD4 |
| Dr.Jucre Rebirth Eye | NIACINAMIDE | NATURECELL CO., LTD. | 2ab43971-57b4-aa2c-e063-6294a90a8f7b | 2025-01-02 | Warnings | 25X51I8RD4 |
| Dr.Jucre Rebirth Booster | NIACINAMIDE | NATURECELL CO., LTD. | 2ab42408-1323-9d79-e063-6394a90a434b | 2025-01-02 | Warnings | 25X51I8RD4 |
| Dr.Jucre Rebirth | NIACINAMIDE, ADENOSINE | NATURECELL CO., LTD. | 2ab449f5-02eb-b075-e063-6394a90a9b50 | 2025-01-02 | Warnings | 25X51I8RD4 |
| Dr.Jucre Rebirth | NIACINAMIDE | NATURECELL CO., LTD. | 2ab4562d-e8b4-c9a4-e063-6394a90ada47 | 2025-01-02 | Warnings | 25X51I8RD4 |
| Dr.Jucre Rebirth Sun Protection | OCTINOXATE, HOMOSALATE, OCTISALATE, AVOBENZONE, ENSULIZOLE, OCTOCRYLENE, BEMOTRIZINOL, NIACINAMIDE, ADENOSINE | NATURECELL CO., LTD. | 2ab49052-085f-024e-e063-6394a90a81b8 | 2025-01-02 | Warnings | 25X51I8RD4 |
| Fendall Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | afda6fc3-7615-b0be-e053-2995a90a6208 | 2024-12-10 | Warnings | 059QF0KO0R |
| Ventrixyl | FOLIC ACID | PureTek Corporation | c29dc729-93be-2a20-e053-2a95a90a8ca3 | 2024-12-03 | Warnings, Adverse reactions | 25X51I8RD4 |
| Folitin-Z | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb141ac2-e5df-4df4-e053-2995a90a6e72 | 2024-12-02 | Warnings, Adverse reactions | 25X51I8RD4 |
| Davimet with Iron | IRON, FOLATE | PureTek Corporation | 1445921b-5bf4-ea48-e063-6294a90abb1a | 2024-11-27 | Warnings, Adverse reactions | 25X51I8RD4 |
| Foliflex | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | cba98d1a-8cf9-39d9-e053-2995a90ae8bb | 2024-11-27 | Warnings, Adverse reactions | 25X51I8RD4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.