NDC 11673-283 - Daytime Nighttime Sinus Relief
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
- 11673-283
- Manufacturer
- Target Corporation | LNK International, Inc.
- Effective date
- 2026-05-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Target 44-615694-09 Delisted | Target Corporation | LNK International, Inc. | 2026-05-18 | 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 |
|---|---|---|---|---|---|---|
| CoTZ Silky Foam Non-Tinted | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD | 9c04b76e-ae65-4183-b475-3b8e8764db59 | 2025-01-24 | Warnings | 15FIX9V2JP |
| Mucus Relief Extended Release | GUAIFENESIN | Redpharm Drug Inc. | f4c1e725-bcae-2255-e053-2995a90ad335 | 2025-01-23 | Warnings | 495W7451VQ |
| good sense pain relief | ACETAMINOPHEN | Preferred Pharmaceuticals Inc. | 523b68da-cd2a-4960-95e7-de5d51ce33c1 | 2025-01-23 | Warnings | 362O9ITL9D |
| PHENYLEPHRINE HYDROCHLORIDE | PHENYLEPHRINE HYDROCHLORIDE | Caplin Steriles Limited | 1b3eec91-5be5-4010-bf92-4c3e72b39b2a | 2025-01-23 | Warnings, Adverse reactions | 04JA59TNSJ |
| DOCTRUST K Tooth | SILICON DIOXIDE, SODIUM MONOFLUOROPHOSPHATE | DOCSMEDI Co., Ltd. | a02f8865-e7be-4ef4-b09c-dad846639764 | 2025-01-22 | Warnings | ETJ7Z6XBU4 |
| Acetaminophen and Codeine Phosphate | ACETAMINOPHEN AND CODEINE PHOSPHATE | Direct_Rx | e78e50c0-36da-528e-e053-2995a90a3d80 | 2025-01-22 | Warnings, Adverse reactions | 362O9ITL9D |
| Tramadol Hydrochloride and Acetaminophen | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | Direct_Rx | e8a7c995-e473-ca87-e053-2995a90a5b80 | 2025-01-22 | Warnings, Adverse reactions | 362O9ITL9D |
| HYDROCODONE/APAP | HYDROCODONE/APAP | Direct_Rx | efe3b2eb-5c26-3783-e053-2995a90a6ba8 | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Percocet | OXYCODONE/APAP | Direct_Rx | ee151649-b52a-0a51-e053-2a95a90a6c35 | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Norco | HYDROCODONE/APAP | Direct_Rx | ee248dfd-7aa7-7dcc-e053-2995a90af19f | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Hydrocodone/APAP | HYDROCODONE/APAP | Direct_Rx | f0e66441-668a-7ab8-e053-2995a90aba4f | 2025-01-22 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Lemon Quince | LEMON QUINCE | Uriel Pharmacy Inc | 332e4a40-e0f3-11de-8a39-0800200c9a66 | 2025-01-22 | Warnings | ETJ7Z6XBU4 |
| Childrens Allergy Relief | DIPHENHYDRAMINE HCL | Best Choice | 0035e6a4-b3ef-4e0b-aa7f-7453dd065f4d | 2025-01-22 | Warnings | TC2D6JAD40 |
| GOOD REMEDIES Allergy Relief SOFTGEL | DIPHENHYDRAMINE HYDROCHLORIDE | Strive Pharmaceuticals Inc. | 26a02737-2cfd-769f-e063-6394a90af352 | 2025-01-22 | Warnings | TC2D6JAD40 |
| PHARBEDRYL | DIPHENHYDRAMINE HCL 50MG | Ulai Health LLC | 135293fb-5674-4638-be55-b968cf51257e | 2025-01-20 | Warnings | TC2D6JAD40 |
| Pharbetol | ACETAMINOPHEN 325 MG | Ulai Health LLC | 55bb7e6c-e98c-48bd-b7bb-9848ff0273ca | 2025-01-20 | Warnings | 362O9ITL9D |
| ACETAMINOPHEN PM | ACETAMINOPHEN 500MG / DIPHENHYDRAMINE HCL 25MG | Ulai Health LLC | d4a568c9-a721-48d1-aebc-fc65444947ce | 2025-01-20 | Warnings | TC2D6JAD40 362O9ITL9D |
| Pharbinex | GUAIFENESIN 400MG | Ulai Health LLC | 4eafa81a-aeee-4c97-85d6-594902b10919 | 2025-01-20 | 495W7451VQ | |
| Pharbinex-PE | GUAIFENESIN 400MG AND PHENYLEPHRINE HCL 10MG | Ulai Health LLC | e459bb83-b1d6-42fc-aa46-99ad117e6144 | 2025-01-20 | 04JA59TNSJ 495W7451VQ | |
| Pharbinex-DM | GUAIFENESIN 400MG AND DEXTROMETHORPHAN HBR 20MG | Ulai Health LLC | af80d10e-3fb2-405a-a803-1f876b8dcd10 | 2025-01-20 | 495W7451VQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.