NDC 50090-7283-01 - Ibuprofen
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
- 50090-7283
- Requested NDC
- 50090-7283-01
- Package NDCs from labels
- 50090-7283-0, 50090-7283-1, 50090-7283-2, 50090-7283-3, 50090-7283-4, 50090-7283-5, 50090-7283-7, 50090-7283-8, 50090-7283-9, 50090-7283-01
- Manufacturer
- A-S Medication Solutions
- Effective date
- 2024-10-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen - A-S Medication Solutions | A-S Medication Solutions | 2024-10-10 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50090-7283-0 | Ibuprofen | 10 in 1 BOTTLE | TABLET, FILM COATED | 10 | 1 | |
| 50090-7283-1 | Ibuprofen | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | 1 | |
| 50090-7283-2 | Ibuprofen | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 1 | |
| 50090-7283-3 | Ibuprofen | 45 in 1 BOTTLE | TABLET, FILM COATED | 45 | 1 | |
| 50090-7283-4 | Ibuprofen | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 1 | |
| 50090-7283-5 | Ibuprofen | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 1 | |
| 50090-7283-7 | Ibuprofen | 21 in 1 BOTTLE | TABLET, FILM COATED | 21 | 1 | |
| 50090-7283-8 | Ibuprofen | 12 in 1 BOTTLE | TABLET, FILM COATED | 12 | 1 | |
| 50090-7283-9 | Ibuprofen | 40 in 1 BOTTLE | TABLET, FILM COATED | 40 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50090-7283 | IBUPROFEN TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, 9 package rows | 20241012_b0917020-f0ec-4d07-8fbf-c1eb909f466b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 50090-7283-0 | EA - Each | 50090-7283 | 7d04ae4a-a5d7-4344-8383-462147929bdf | 1 | 2024-11-05 |
| 50090-7283-1 | EA - Each | 50090-7283 | bdca7862-c9a3-429b-91b1-962064ba4616 | 1 | 2024-11-05 |
| 50090-7283-2 | EA - Each | 50090-7283 | 6199b073-54e2-426a-a97c-47cdc0cdaea4 | 1 | 2024-11-05 |
| 50090-7283-3 | EA - Each | 50090-7283 | bac64cb4-6642-4ad4-8b18-3c58532178ad | 1 | 2024-11-05 |
| 50090-7283-4 | EA - Each | 50090-7283 | da21a1ed-e009-4529-8d94-c71d1bb7ff0d | 1 | 2024-11-05 |
| 50090-7283-5 | EA - Each | 50090-7283 | b5cd512c-f12f-492f-b333-b5bde741850c | 1 | 2024-11-05 |
| 50090-7283-7 | EA - Each | 50090-7283 | 4cb37eb8-46f6-4e17-b17d-d4fcd39cc057 | 1 | 2024-11-05 |
| 50090-7283-8 | EA - Each | 50090-7283 | 423911b6-ba17-4535-a9ec-ace0998efe86 | 1 | 2024-11-05 |
| 50090-7283-9 | EA - Each | 50090-7283 | 60feb7e1-4517-4588-8964-fa97f5223739 | 1 | 2024-11-05 |
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 |
|---|---|---|---|---|---|---|
| Ibuprofen | IBUPROFEN | P & L Development, LLC | 159b68b7-54e5-4f83-b632-f49e7b4b14a5 | 2026-08-05 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Walgreen Company | c118b290-f821-4e73-906e-8a93edaf34e4 | 2026-08-05 | Warnings | WK2XYI10QM |
| Dye Free Ibuprofen | IBUPROFEN | Walgreen Company | 8944a0e8-2928-4494-915f-d1e0a6d4bf5c | 2026-08-04 | Warnings | WK2XYI10QM |
| ROROBELL WAWA Whitening Tooth | SILICA, HYDROGEN PEROXIDE, TOCOPHERYL ACETATE | ROROBELL | 58336a0d-49dd-ef13-e063-6394a90a38c1 | 2026-08-04 | Warnings | ETJ7Z6XBU4 |
| Ibuprofen | IBUPROFEN | REMEDYREPACK INC. | 560e4e05-21e0-4b2a-ab2f-872b5dbb3901 | 2026-08-04 | Boxed warning, Warnings, Adverse reactions | 197807 WK2XYI10QM |
| Silicea 6X | SILICON DIOXIDE | Hyland's Inc. | db4be3c1-aa7e-24a2-e053-2a95a90a0c66 | 2026-08-04 | Warnings | ETJ7Z6XBU4 |
| Ibuprofen | IBUPROFEN | Chain Drug Marketing Association, Inc. | 733d0b21-c177-4c60-9243-2f1e7cb5854a | 2026-08-04 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Pioneer Life Sciences, LLC | 8abd74a4-ad33-4c10-b677-acb469f815e6 | 2026-08-03 | Warnings | WK2XYI10QM |
| Ibuprofen | IBUPROFEN | Pioneer Life Sciences, LLC | 291602fa-8ebe-4200-bba7-9798c90f8a50 | 2026-08-03 | Warnings | WK2XYI10QM |
| Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY | OCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8% | Lale Cosmetics LLC | 581fb0cd-c55d-d562-e063-6394a90a7f11 | 2026-08-03 | Warnings | 15FIX9V2JP |
| Ibuprofen | IBUPROFEN | NUVICARE LLC | b063d2dc-d579-46e7-8cfc-1596c803c7f9 | 2026-08-03 | Warnings | WK2XYI10QM |
| EltaMD UV Active | ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN | CP Skin Health Group, Inc | 39d16479-d491-4c19-aa11-674461687c7b | 2026-08-03 | Warnings | 15FIX9V2JP |
| Ibuprofen | IBUPROFEN | NUVICARE LLC | 7905edc1-2a45-4adc-a7bc-42b1ddb6ba59 | 2026-08-03 | Warnings | WK2XYI10QM |
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Doc Rx | 9f5de6af-e555-4efd-a3ed-b72c34c051b6 | 2026-08-01 | Boxed warning, Warnings, Adverse reactions | WK2XYI10QM |
| Ibuprofen and Pseudoephedrine Hydrochloride | IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE | Rite-Aid | 483c3bb7-529e-4684-80e1-6646b050988e | 2026-07-31 | Warnings | WK2XYI10QM |
| Ibuprofen and Pseudoephedrine Hydrochloride | IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE | Publix Super Markets Inc | 2b98a62b-bd92-4fb8-ad0f-521cb477b612 | 2026-07-31 | Warnings | WK2XYI10QM |
| Continuous Correction Cream | TITANIUM DIOXIDE | Baxter of California, LLC | 1cbcc648-f2e1-af60-e063-6294a90ad4bb | 2026-07-31 | Warnings | 15FIX9V2JP |
| Cover Creme | TITANIUM DIOXIDE | Baxter of California | 31f5e8c4-523f-4596-e063-6294a90a6a12 | 2026-07-31 | Warnings | 15FIX9V2JP |
| Smogstat | ECHINACEA (ANGUSTIFOLIA), HYPERICUM PERFORATUM, HYDRASTIS CANADENSIS, SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, CARBO VEGETABILIS, CAUSTICUM, KALI CARBONICUM, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SILICEA | Energique, Inc. | 59f63e2b-24fa-43a0-8334-02e6729c6ac1 | 2026-07-31 | Warnings | ETJ7Z6XBU4 |
| Muscle Ice | PHYTOLACCA DECANDRA, BELLIS PERENNIS, LEDUM PALUSTRE, RUTA GRAVEOLENS, SYMPHYTUM OFFICINALE, MAGNESIA PHOSPHORICA, SILICEA, MENTHOL (CRYSTALS) | Peaceful Mountain, Inc. | 03b6e2a9-f335-4ae2-9011-80bd019afb72 | 2026-07-30 | Warnings | ETJ7Z6XBU4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.