NDC 85237-1955-01 - Tylenol Sinus Severe
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
- 85237-1955
- Requested NDC
- 85237-1955-01
- Package NDCs from labels
- 85237-1955-0, 85237-1955-1, 85237-1955-2, 85237-1955-3, 85237-1955-4, 85237-1955-6, 85237-1955-7, 85237-1955-01
- Manufacturer
- Select Consumer Group LLC | Select Consumer Group
- Effective date
- 2026-05-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Tylenol Sinus Severe - Select Consumer Group LLC | Select Consumer Group | Select Consumer Group LLC | Select Consumer Group | 2026-05-27 | 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.
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| VEIL MINERAL PRIMER SUNSCREEN BROAD SPECTRUM SPF 15 | ZINC OXIDE AND TITANIUM DIOXIDE | Kingdom Animalia, LLC DBA Hourglass Cosmetics | 28e23498-953f-47c0-838c-bbf0e858d903 | 2025-11-24 | Warnings | 15FIX9V2JP |
| Throat Coat Eucalyptus Mint | MENTHOL | Traditional Medicinals, Inc. | a7a86f1b-30e8-6f5d-e053-2a95a90a2a82 | 2025-11-21 | Warnings | M012 |
| Throat Coat Sweet Orange Fennel | MENTHOL | Traditional Medicinals, Inc. | 4538248f-11cc-d6b2-e063-6294a90a652c | 2025-11-21 | Warnings | M012 |
| Childrens Multi-symptom Cold Daytime | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Wal-Mart Stores, Inc. | 1768677d-96ec-f9f7-e063-6394a90a4ef4 | 2025-11-21 | Warnings | 04JA59TNSJ 495W7451VQ |
| MUCUS RELIEF MAX | GUAIFENESIN | Better Living Brands, LLC | 8b981962-5724-47d0-81f5-945dea169943 | 2025-11-21 | Warnings | 495W7451VQ |
| up and up Daytime Nighttime Childrens Multi Symptom Cold | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DIPHENHYDRAMINE HYDROCHLORIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Target Corporation | b8a4da0b-e4d3-48e6-b699-cb56c7b67ed7 | 2025-11-20 | Warnings | M012 |
| Mucus Relief | GUAIFENESIN | AMERIFOODS TRADING COMPANY | 3802d63d-7dba-50de-e063-6294a90acf7b | 2025-11-20 | Warnings | 495W7451VQ |
| Arthritis Pain | ACETAMINOPHEN | AMERIFOODS TRADING COMPANY | 3802bc07-3154-f36a-e063-6294a90ac1cc | 2025-11-20 | Warnings | 362O9ITL9D |
| SULWHASOO PERFECTING CUSHION NO. 15 | OCTINOXATE, TITANIUM DIOXIDE, AND ZINC OXIDE | Amorepacific Corporation | 8d420e4b-c778-3ed4-e053-2995a90a59a9 | 2025-11-20 | Warnings | 15FIX9V2JP |
| Protect Prevent Daily Mineral Sunscreen Broad Spectrum SPF30 | TITANIUM DIOXIDE, ZINC OXIDE | Norwex Usa, Inc. | f527a8c5-b05e-5f3c-e053-2995a90aa1a3 | 2025-11-20 | Warnings | 15FIX9V2JP |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 4227aeb1-dd2c-9ca1-e063-6294a90ad709 | 2025-11-20 | Warnings | 362O9ITL9D |
| good sense pain relief | ACETAMINOPHEN | NuCare Pharamceuticals, Inc. | 440c13d7-edf0-f611-e063-6394a90af995 | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 42394377-c874-a955-e063-6294a90ace0b | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 4227a2cc-69fa-869d-e063-6294a90a1d41 | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 422796ed-7558-f7e8-e063-6294a90ad1c7 | 2025-11-20 | Warnings | 362O9ITL9D |
| Arthritis Pain | ACETAMINOPHEN | HYVEE INC | 3e61b583-c1cb-23bd-e063-6294a90aa006 | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief | ACETAMINOPHEN | HYVEE INC | 3e61abe4-b4be-01af-e063-6394a90a8b24 | 2025-11-20 | Warnings | 362O9ITL9D |
| Pain Relief PM | ACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE | HYVEE INC | 3e60703b-a5cf-333a-e063-6394a90a2087 | 2025-11-20 | Warnings | 362O9ITL9D |
| Supress DX Pediatric Drops | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | KRAMER NOVIS | ddb95436-7806-4086-af4d-18a6625b5c83 | 2025-11-20 | Warnings | M012 04JA59TNSJ 495W7451VQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.