NDC 50488-0901-01 - Laxacin
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
- 50488-0901
- Requested NDC
- 50488-0901-01
- Package NDCs from labels
- 50488-0901-1, 50488-0901-01
- Manufacturer
- Advanced Rx Pharmacy of Tennessee, LLC
- Effective date
- 2024-12-31
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Laxacin - Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennessee, LLC | 2024-12-31 | HUMAN OTC DRUG LABEL |
| Laxacin - Alexso, Inc | Alexso, Inc | 2024-12-04 | HUMAN OTC DRUG LABEL |
| Laxacin - Quality Care Products, LLC | Quality Care Products, LLC | 2023-12-21 | HUMAN OTC DRUG LABEL |
| LAXACIN - Direct_Rx | Direct_Rx | 2023-10-06 | HUMAN OTC DRUG LABEL |
| Laxacin Laxative Plus Stool Softener | NuCare Pharmaceuticals,Inc. | 2021-02-11 | HUMAN OTC DRUG LABEL |
| Laxacin - medsource pharmaceuticals | medsource pharmaceuticals | 2018-12-20 | HUMAN OTC DRUG LABEL |
| LAXACIN - DIRECT RX | DIRECT RX | 2018-03-26 | HUMAN OTC DRUG LABEL |
| Laxacin Laxative Plus Stool Softener | Dispensing Solutions, Inc. | PSS World Medical, Inc. | 2013-07-12 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50488-0901-1 | Laxacin | 100 in 1 BOTTLE | TABLET | 100 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50488-0901 | LAXACIN (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ALEXSO, INC] | 8 | Current NDC, Legacy NDC, 1 package rows | 20241208_0df9abaf-3997-4dde-8003-ae3d8d07cf39.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50488-0901-1 | EA - Each | 50488-0901 | 933d71c3-b01d-44ff-b256-0bee20827ae8 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| D-133 | CALCIUM FLUORIDE, SILICON DIOXIDE, TRIBASIC CALCIUM PHOSPHATE, CALCIUM SULFATE ANHYDROUS, FERROSOFERRIC PHOSPHATE, POTASSIUM CHLORIDE, DIBASIC POTASSIUM PHOSPHATE, POTASSIUM SULFATE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, SODIUM CHLORIDE, AND SODIUM SULFATE | DNA Labs, Inc. | a250b7e9-7fd2-4cb0-82f3-baa089d17441 | 2025-01-13 | Warnings | ETJ7Z6XBU4 |
| Brush and Go All Skin types | TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE | Noon Aesthetics M.R. Ltd | 9ee5b3c2-4369-4c4b-ab55-b52661b82188 | 2025-01-13 | Warnings | 15FIX9V2JP |
| Priia Tinted Mineral Sunscreen and Primer | TITANIUM DIOXIDE, ZINC OXIDE | Priia Cosmetics Inc | 5c4219ac-d65f-43a5-8ec4-8732b9b344cf | 2025-01-13 | Warnings | 15FIX9V2JP |
| Brush and Go Oily Problematic Skin | TITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE, AND OXYBENZONE | Noon Aesthetics M.R. Ltd | b4295453-f193-4bed-be5b-efcd91772107 | 2025-01-13 | Warnings | 15FIX9V2JP |
| Priia Tinted Mineral Sunscreen and Primer | TITANIUM DIOXIDE, ZINC OXIDE | Priia Cosmetics Inc | b2addf27-9139-48b4-85e6-618f4b5311cc | 2025-01-13 | Warnings | 15FIX9V2JP |
| SUN PROTECT LIP BALM SPF 30 | ZINC OXIDE AND TITANIUM DIOXIDE | Stream2Sea, LLC | 21386652-b952-48be-b077-1acecc7f0eb0 | 2025-01-12 | Warnings | 15FIX9V2JP |
| Senna-S | SENNOSIDES 8.6MG AND DOCUSATE SODIUM 50MG | Ulai Health LLC | c0e27b02-8ef2-4239-8f8c-790f7d978dc0 | 2025-01-12 | Warnings | M007 998740 F05Q2T2JA0 |
| Dermaroller Anhydrous Sunscreen SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | Owen Biosciences, Inc. | 04e82f1b-c893-4795-b7a9-0523e3ec7552 | 2025-01-10 | Warnings | 15FIX9V2JP |
| Aurum Hypericum | AURUM HYPERICUM | Uriel Pharmacy Inc | be0da1f0-06a1-11df-8a39-0800200c9a66 | 2025-01-10 | Warnings | ETJ7Z6XBU4 |
| Docusate Sodium | DOCUSATE SODIUM | Major Pharmaceuticals | 1541ff5b-11f8-444b-a2a0-8e3086ae650a | 2025-01-10 | Warnings | M007 F05Q2T2JA0 |
| Docusate Sodium | DOCUSATE SODIUM | AvPAK | f31a4349-7826-45c0-9388-6b938d167b7a | 2025-01-09 | Warnings | M007 F05Q2T2JA0 |
| Protect Tinted Mineral Sunscreen Broad Spectrum SPF 30 | TITANIUM DIOXIDE AND ZINC OXIDE | NEW SEASON DERMATOLOGY, PLLC | fecd72a3-c7e5-3dfa-e053-6394a90a7357 | 2025-01-09 | Warnings | 15FIX9V2JP |
| Docusate sodium | DOCUSATE SODIUM | APNAR PHARMA LP | 05b0732b-012f-78ee-e063-6294a90a839a | 2025-01-09 | Warnings | M007 F05Q2T2JA0 |
| ECLIPSE SPF 50 PERFECTINT BEIGE | TITANIUM DIOXIDE, ZINC OXIDE | SCIENCE OF SKINCARE LLC | b69dda25-372f-15d9-e053-2995a90a8d3e | 2025-01-09 | Warnings | 15FIX9V2JP |
| Extreme Protect SPF 40 All Shades | ZINC OXIDE, TITANIUM DIOXIDE | Science of Skincare, LLC. | b69db78b-5f0e-8ca2-e053-2a95a90ac88c | 2025-01-09 | Warnings | 15FIX9V2JP |
| ECLIPSE SPF 50 ALL SHADES | TITANIUM DIOXIDE, ZINC OXIDE | SCIENCE OF SKINCARE LLC | 49df51e6-be9a-41be-b3e1-bfc062aaceaa | 2025-01-09 | Warnings | 15FIX9V2JP |
| AM-9 | SPIGELIA ANTHELMIA, SILICON DIOXIDE, AND CORALLIUM RUBRUM WHOLE | DNA Labs, Inc. | d7a00f0b-de4c-4bff-b8e0-86a82bed8bb9 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-8 | SILICON DIOXIDE, ATROPA BELLADONNA, CITRULLUS COLOCYNTHIS FRUIT PULP, BLACK COHOSH, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, PALLADIUM, APIS MELLIFERA, AND BOS TAURUS OVARY | DNA Labs, Inc. | c25cdcb5-9469-48bb-b216-0a9d8d644e12 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-23 | ANEMONE PULSATILLA, PHOSPHORUS, SILICON DIOXIDE, NITRIC ACID, ARSENIC TRIOXIDE, TOXICODENDRON PUBESCENS WHOLE, AND BOS TAURUS HYPOTHALAMUS | DNA Labs, Inc. | b6365b49-06fb-4692-96f7-a5097b70bc91 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
| N-16 | MGO ENERGIZER | DNA Labs, Inc. | 8292b900-86c1-47ea-81da-b587439c7664 | 2025-01-09 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.