NDC 71474-301 - keragel
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
- 71474-301
- Package NDCs from labels
- 71474-301-20, 71474-301-10, 71474-301-30, 71474-301-55, 71474-301-05
- Manufacturer
- MOLECULAR BIOLOGICALS, LLC
- Effective date
- 2018-09-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| keragel - MOLECULAR BIOLOGICALS, LLC | MOLECULAR BIOLOGICALS, LLC | 2018-09-26 | PRESCRIPTION MEDICAL DEVICE LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71474-301-05 | keragel | 5 g in 1 TUBE | 5 | 6 | ||
| 71474-301-05 | keragel | 1 in 1 BOX | 1 | 6 | ||
| 71474-301-10 | keragel | 20 g in 1 TUBE | 20 | 6 | ||
| 71474-301-10 | keragel | 10 in 1 BOX | 10 | 6 | ||
| 71474-301-20 | keragel | 1 in 1 BOX | 1 | 6 | ||
| 71474-301-20 | keragel | 20 g in 1 TUBE | 20 | 6 | ||
| 71474-301-30 | keragel | 20 g in 1 TUBE | 20 | 6 | ||
| 71474-301-30 | keragel | 30 in 1 BOX | 30 | 6 | ||
| 71474-301-55 | keragel | 5 in 1 BOX | 5 | 6 | ||
| 71474-301-55 | keragel | 20 g in 1 TUBE | 20 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71474-301-05 | GM - Gram | 71474-301 | ef510378-67fc-4f96-a667-262a03d214bc | 1 | 2021-12-08 |
| 71474-301-10 | GM - Gram | 71474-301 | 4b5fb54d-8433-4753-8014-93fd4f5a081d | 1 | 2017-08-11 |
| 71474-301-20 | GM - Gram | 71474-301 | aac6587d-5438-4c87-8a7a-088ac89a2522 | 1 | 2017-08-11 |
| 71474-301-30 | GM - Gram | 71474-301 | dc37793f-0ec7-49d8-baf4-0bf2ad61a465 | 1 | 2017-08-11 |
| 71474-301-55 | GM - Gram | 71474-301 | 19b328a8-e99c-411c-ba95-8709c3ede329 | 1 | 2017-11-06 |
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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| ANTIBACTERIAL DREAMY FLORALS | GLYCERIN | Quimicas Handal de Centroamerica SA de CV | 09f73bec-516d-90f0-e063-6394a90aecab | 2025-01-08 | Warnings | PDC6A3C0OX |
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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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| OASIS Tears Preservative-Free Lubricant Eye | GLYCERIN | OASIS Medical, Inc. | d9d71b1d-82a6-42e7-9ef2-2d041daef936 | 2024-12-23 | Warnings | PDC6A3C0OX |
| 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 |
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| Stratuscare Adult Glycerin | GLYCERIN | Stratus Pharmaceuticals | 3e1935da-5c1f-4942-98dd-320fade82321 | 2024-11-04 | Warnings | PDC6A3C0OX |
| Stratuscare Glycerin Laxative Pediatric | GLYCERIN | Stratus Pharmaceuticals | 6ae6d3c4-bb3b-4436-b76d-8654bf871e66 | 2024-11-01 | Warnings | PDC6A3C0OX |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.