NDC 69153-080-01 - AN ADC SP INTENSIVE MOISTURE ESSENCE
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
- 69153-080
- Requested NDC
- 69153-080-01
- Package NDCs from labels
- 69153-080-01, 69153-080-02
- Manufacturer
- AN Co Ltd.
- Effective date
- 2016-06-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| AN ADC SP INTENSIVE MOISTURE ESSENCE - AN Co Ltd. | AN Co Ltd. | 2016-06-24 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69153-080-02 | 2023-01-30 | C162847 | 48780-1 | f386c649-bed8-0266-e053-dadaa90a7c1a | 80861d31-100a-4c97-b9c7-afc3d8b3371a |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 69153-080-01 | AN ADC SP INTENSIVE MOISTURE ESSENCE | 55 g in 1 BOTTLE, PUMP | CREAM | 55 | 1 | |
| 69153-080-02 | AN ADC SP INTENSIVE MOISTURE ESSENCE | 1 in 1 CARTON | CREAM | 1 | 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 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 |
| PhysiciansCare Ophthalmic Solution Eyewash Purified Water, 98.3% | PURIFIED WATER 98.3% | Acme United Corporation | 9248ee71-2d47-620d-e053-2995a90af5c8 | 2024-11-26 | Warnings | 059QF0KO0R |
| PhysiciansCare Ophthalmic Solution Eyewash | PURIFIED WATER 98.3% | Acme United Corporation | cca454e0-b2bd-4215-bc06-426fcc3f7bd6 | 2024-11-26 | Warnings | 059QF0KO0R |
| PhysiciansCare Ophthalmic Solution Eyewash | PURIFIED WATER 98.3% | Acme United Corporation | d3812fa3-9334-464d-b50c-98548ff76727 | 2024-11-26 | Warnings | 059QF0KO0R |
| DANGTTEOL | MINERAL WATER | AQBC CO., LTD | 27db14a9-3812-433f-e063-6394a90a11e7 | 2024-11-26 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.