NDC 84067-666-01 - liquid
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
- 84067-666
- Requested NDC
- 84067-666-01
- Package NDCs from labels
- 84067-666-01
- Manufacturer
- Shantou Youjia E-Commerce Co., Ltd.
- Effective date
- 2024-05-04
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OUHOE Botox Facial Essence | Shantou Youjia E-Commerce Co., Ltd. | 2024-05-04 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 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 |
| Crane Safety Eye Wash | WATER SOLUTION | Crane Safety LLC | 96d8dda9-6cd6-3f68-e053-2995a90a0da2 | 2024-11-08 | Warnings | 059QF0KO0R |
| RUGBY EYE WASH | WATER, PURIFIED | A-S Medication Solutions | 0773e558-2f46-494c-888a-3bc517202b65 | 2024-11-08 | Warnings | 059QF0KO0R |
| Finazol | FERROUS FUMARATE, FOLATE | PureTek Corporation | 24290823-022a-433b-e063-6394a90a8fd0 | 2024-11-07 | Warnings, Adverse reactions | 25X51I8RD4 |
| EyeOne eyelid cleansing tools | HYALURONIC ACID | IDO PHARM | cba8f11b-3aeb-46c1-ad2a-7d2535cb1166 | 2024-10-15 | Warnings | S270N0TRQY |
| EyS Eye Wash | WATER | Eyes-Plus LLC | 1443f6bf-3a77-4a19-8585-0ec58efe042f | 2024-10-15 | Warnings | 059QF0KO0R |
| Eye Wash | WATER SOLUTION | Kroger Company | 354402ad-581d-47e7-9fd3-933bef281ff4 | 2024-10-11 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.