NDC 72044-102-01 - CELDERMA Ninetalks Hydrogel Eye Patch
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
- 72044-102
- Requested NDC
- 72044-102-01
- Package NDCs from labels
- 72044-102-01, 72044-102-02
- Manufacturer
- GENIC CO., LTD
- Effective date
- 2018-03-20
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CELDERMA Ninetalks Hydrogel Eye Patch - GENIC CO., LTD | GENIC CO., LTD | 2018-03-20 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72044-102-02 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-343d-a426-e053-dadaa90af4c2 | CELDERMA Ninetalks Hydrogel Eye Patch |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72044-102-01 | CELDERMA Ninetalks Hydrogel Eye Patch | 4.7 g in 1 PATCH | PATCH | 4.7 | 1 | |
| 72044-102-02 | CELDERMA Ninetalks Hydrogel Eye Patch | 1 in 1 POUCH | PATCH | 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.
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| Dr.Jucre Rebirth | NIACINAMIDE | NATURECELL CO., LTD. | 2ab4562d-e8b4-c9a4-e063-6394a90ada47 | 2025-01-02 | Warnings | 25X51I8RD4 |
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| CLENZIDERM THERAPEUTIC MOISTURIZER | GLYCERIN | Obagi Cosmeceuticals LLC | d60e22e3-831e-4787-a82c-e7763c287553 | 2025-01-01 | Warnings | PDC6A3C0OX |
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| Tucks Triple Relief Hemorrhoidal | WHITE PETROLATUM, GLYCERIN, PRAMOXINE HYDROCHLORIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Blistex Inc. | bf892e90-2d9b-4fa0-8ee4-8a2736be6c30 | 2024-12-24 | Warnings | PDC6A3C0OX |
| Pedia-Lax | GLYCERIN | C.B. Fleet Company, Inc. | 4e15f6ca-a40c-485f-be3f-07c2ed7cb498 | 2024-12-23 | Warnings | PDC6A3C0OX |
| OASIS Tears Preservative-Free Lubricant Eye | GLYCERIN | OASIS Medical, Inc. | d9d71b1d-82a6-42e7-9ef2-2d041daef936 | 2024-12-23 | Warnings | PDC6A3C0OX |
| DCH Scar | ALLANTOIN 0.5% | Derma Care Research Labs, LLC | 00edbc64-9d32-5751-e063-6294a90a400b | 2024-12-19 | Warnings | 344S277G0Z |
| DCH Hemorrhoidal | GLYCERIN 14.4%, LIDOCAINE 5%, PETROLATUM 15%, PHENYLEPHRINE HCL 0.25% | Derma Care Research Labs, LLC | 0050701f-4393-3f01-e063-6394a90a4e0e | 2024-12-19 | Warnings | PDC6A3C0OX |
| Revivol Hemorrhoid and Fissure | GLYCERIN 14.4%, LIDOCAINE 5%, PETROLATUM 15%, PHENYLEPHRINE HCL 0.25% | Derma Care Research Labs, LLC | 0140cf68-b6a0-4378-e063-6394a90afee8 | 2024-12-19 | Warnings | PDC6A3C0OX |
| RECTICARE | LIDOCAINE AND GLYCERIN | Ferndale Laboratories, Inc. | 2b94136a-4975-2925-e054-00144ff88e88 | 2024-12-17 | Warnings | PDC6A3C0OX |
| Adenosine | ADENOSINE | Medical Purchasing Solutions, LLC | 296af833-5724-3e23-e063-6394a90a6251 | 2024-12-16 | Warnings, Adverse reactions | K72T3FS567 |
| QC Scar | ALLANTOIN 0.5% | CDMA | f7e3d751-a47a-2bca-e053-6394a90a6541 | 2024-12-15 | Warnings | 344S277G0Z |
| Fendall Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | afda6fc3-7615-b0be-e053-2995a90a6208 | 2024-12-10 | Warnings | 059QF0KO0R |
| SOOTHE Sensitive Skin Treatment | ALLANTOIN, DIMETHICONE | Rodan & Fields | 2bd8cac4-5f40-4d04-91f2-3ea8a138033b | 2024-12-09 | Warnings | 344S277G0Z |
| adenosine | ADENOSINE | Sagent Pharmaceuticals | 5a55b45d-9cee-4c0c-9e44-021dbf70a018 | 2024-12-04 | Warnings, Adverse reactions | K72T3FS567 |
| Burts Bees Rapid Rescue Cold Sore Treatment | CAMPHOR, GLYCERIN | Burts Bees | 9f89735d-205f-4d3e-a1e1-ecc96284fe98 | 2024-12-03 | Warnings | PDC6A3C0OX |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.