NDC 50580-449-07 - TYLENOL Extra Strength
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
- 50580-449
- Requested NDC
- 50580-449-07
- Package NDCs from labels
- 50580-449-00, 50580-449-05, 50580-449-08, 50580-449-09, 50580-449-10, 50580-449-11, 50580-449-13, 50580-449-14, 50580-449-15, 50580-449-23, 50580-449-31, 50580-449-34, 50580-449-35, 50580-449-36, 50580-449-61, 50580-449-62, 50580-449-84, 50580-449-85, 50580-449-86, 50580-449-87, 50580-449-12, 50580-449-96, 50580-449-97, 50580-449-98, 50580-449-66, 50580-449-37, 50580-449-07
- Manufacturer
- Select Consumer Group LLC
- Effective date
- 2026-06-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TYLENOL Extra Strength - Select Consumer Group LLC | Select Consumer Group LLC | 2026-06-27 | HUMAN OTC DRUG LABEL |
| TYLENOL Extra Strength - Kenvue Brands LLC | Kenvue Brands LLC | 2026-06-15 | HUMAN OTC DRUG LABEL |
| Tylenol Extra Strength | JC World Bell Wholesale Co., Inc. | McNeil Healthcare LLC | Kenvue Brands LLC | 2026-05-20 | HUMAN OTC DRUG LABEL |
| Tylenol Extra Strength - Savings Distributors LLC | Savings Distributors LLC | 2026-05-01 | HUMAN OTC DRUG LABEL |
| Johnson and Johnson All Purpose First Aid Kit - Kenvue Brands LLC | Kenvue Brands LLC | 2025-11-06 | HUMAN OTC DRUG LABEL |
| Johnson and Johnson First Aid All Purpose 160 CT - Kenvue Brands LLC | Kenvue Brands LLC | 2025-11-06 | HUMAN OTC DRUG LABEL |
| Johnson and Johnson First Aid Travel Ready 80 CT - Kenvue Brands LLC | Kenvue Brands LLC | 2025-11-06 | HUMAN OTC DRUG LABEL |
| TYLENOL Extra Strength - Morning Star OTC | Morning Star OTC | 2025-06-19 | HUMAN OTC DRUG LABEL |
| Tylenol Extra Strength | Navajo Manufacturing Company Inc. | 2024-10-02 | HUMAN OTC DRUG LABEL |
| TYLENOL EXTRA STRENGTH - A-S Medication Solutions | A-S Medication Solutions | 2024-05-16 | HUMAN OTC DRUG LABEL |
| Tylenol Extra Strength | Navajo Manufacturing Company Inc. | Navajo Manufacutring Company Inc. | 2024-04-15 | HUMAN OTC DRUG LABEL |
| ACETAMINOPHEN - JC World Bell Wholesale Co., Inc. | McNeil Healthcare LLC | JC World Bell Wholesale Co., Inc. | McNeil Healthcare LLC | 2023-11-05 | HUMAN OTC DRUG LABEL |
| Tylenol Extra Strength - Select Corporation | Select Corporation | 2022-03-25 | HUMAN OTC DRUG LABEL |
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50580-449-00 | TYLENOL Extra Strength | 125 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 125 | 23 | |
| 50580-449-00 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-05 | TYLENOL Extra Strength | 24 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 24 | 23 | |
| 50580-449-05 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-08 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-09 | TYLENOL Extra Strength | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 23 | |
| 50580-449-09 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-10 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-10 | TYLENOL Extra Strength | 50 in 1 TRAY | TABLET, FILM COATED | 50 | 23 | |
| 50580-449-11 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-11 | TYLENOL Extra Strength | 50 in 1 TRAY | TABLET, FILM COATED | 50 | 23 | |
| 50580-449-12 | TYLENOL Extra Strength | 10 in 1 VIAL, PLASTIC | TABLET, FILM COATED | 10 | 23 | |
| 50580-449-12 | TYLENOL Extra Strength | 12 in 1 PACKAGE | TABLET, FILM COATED | 12 | 23 | |
| 50580-449-13 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-13 | TYLENOL Extra Strength | 3 in 1 CARTON | TABLET, FILM COATED | 3 | 23 | |
| 50580-449-14 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-15 | TYLENOL Extra Strength | 10 in 1 VIAL, PLASTIC | TABLET, FILM COATED | 10 | 23 | |
| 50580-449-23 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-23 | TYLENOL Extra Strength | 150 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 150 | 23 | |
| 50580-449-31 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-31 | TYLENOL Extra Strength | 36 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 36 | 23 | |
| 50580-449-34 | TYLENOL Extra Strength | 325 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 325 | 23 | |
| 50580-449-35 | TYLENOL Extra Strength | 24 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 24 | 23 | |
| 50580-449-35 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-36 | TYLENOL Extra Strength | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | 23 | |
| 50580-449-36 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-37 | TYLENOL Extra Strength | 320 in 1 BOTTLE | TABLET, FILM COATED | 320 | 23 | |
| 50580-449-61 | TYLENOL Extra Strength | 225 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 225 | 23 | |
| 50580-449-61 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-62 | TYLENOL Extra Strength | 325 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 325 | 23 | |
| 50580-449-66 | TYLENOL Extra Strength | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 23 | |
| 50580-449-66 | TYLENOL Extra Strength | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-84 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-85 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-85 | TYLENOL Extra Strength | 50 in 1 TRAY | TABLET, FILM COATED | 50 | 23 | |
| 50580-449-86 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-86 | TYLENOL Extra Strength | 50 in 1 TRAY | TABLET, FILM COATED | 50 | 23 | |
| 50580-449-87 | TYLENOL Extra Strength | 3 in 1 CARTON | TABLET, FILM COATED | 3 | 23 | |
| 50580-449-87 | TYLENOL Extra Strength | 2 in 1 POUCH | TABLET, FILM COATED | 2 | 23 | |
| 50580-449-96 | TYLENOL Extra Strength | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 23 | |
| 50580-449-96 | TYLENOL Extra Strength | 50 in 1 BOTTLE | TABLET, FILM COATED | 50 | 23 | |
| 50580-449-97 | TYLENOL Extra Strength | 249 in 1 PACKAGE, COMBINATION | TABLET, FILM COATED | 249 | 23 | |
| 50580-449-98 | TYLENOL Extra Strength | 110 in 1 PACKAGE, COMBINATION | TABLET, FILM COATED | 110 | 23 | |
| 50580-449-08 | Johnson and Johnson All Purpose First Aid Kit | 2 in 1 POUCH | TABLET, FILM COATED | 4 | 500 mg | 7 |
| 50580-449-08 | Johnson and Johnson First Aid All Purpose160 CT | 2 in 1 POUCH | TABLET, FILM COATED | 4 | 500 mg | 3 |
| 50580-449-08 | Johnson and Johnson First Aid Travel Ready80 CT | 2 in 1 POUCH | TABLET, FILM COATED | 4 | 500 mg | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 50580-449 | TYLENOL EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [KENVUE BRANDS LLC] | 22 | Current NDC, Legacy NDC, 43 package rows | 20250221_59773893-09a8-47a2-943a-e9ea9da4458a.zip |
| 50580-449 | JOHNSON AND JOHNSON ALL PURPOSE FIRST AID KIT (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE) KIT [KENVUE BRANDS LLC] | 6 | Current NDC, Legacy NDC | 20241116_5cdb47c5-7951-4279-8a05-0a3199d3dd45.zip |
| 50580-449 | JOHNSON AND JOHNSON FIRST AID ALL PURPOSE 160 CT (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE) KIT [KENVUE BRANDS LLC] | 2 | Current NDC, Legacy NDC | 20241116_f3933330-2550-4a88-e053-2a95a90a3997.zip |
| 50580-449 | JOHNSON AND JOHNSON FIRST AID TRAVEL READY 80 CT (ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE) KIT [KENVUE BRANDS LLC] | 2 | Current NDC, Legacy NDC | 20241116_f388f105-48ba-4616-e053-2a95a90a0049.zip |
DailyMed Billing Units#
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 |
|---|---|---|---|---|---|---|
| Daytime Sinus Severe | ACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINE HCL | Kroger Company | 1022767d-a456-4fbc-95cf-91337c74c330 | 2026-10-01 | Warnings | 362O9ITL9D |
| Pharmacys Prescription 4.5 OZ Creamy Petroleum Jelly | WHITE PETROLATUM | American Consumer Products Corp. | 5c3eb6b1-d570-0b4c-e063-6394a90af462 | 2026-09-24 | Warnings | 4T6H12BN9U |
| COLTALIN-DM | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE | FORTUNE PHARMACAL COMPANY LIMITED | 33e1bec0-323b-40b7-809a-cb65a71ad0ce | 2026-09-17 | Warnings | 362O9ITL9D |
| JenGufun LIDOCAINE KNEE Patch | LIDOCAINE KNEE PATCH | Henan Kangdi Medical Devices Co., Ltd. | 5b1d8508-b993-7a8d-e063-6294a90ae306 | 2026-09-10 | Warnings | M017 |
| Cold and Flu HBP | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE | Kroger Company | fd41e4a4-330f-4409-8ba3-0b3bb6f45bca | 2026-09-10 | Warnings | 362O9ITL9D |
| Nighttime Sleep Aid Berry Flavor | DIPHENHYDRAMINE HYDROCHLORIDE | Raritan Pharmaceuticals Inc | 303d7651-9c8f-4a14-9f2c-7181fa0f003e | 2026-09-09 | Warnings | TC2D6JAD40 |
| childrens fever reducer and pain reliever | ACETAMINOPHEN | Rite Aid Corporation | 7f445de3-30cf-4bd8-892d-05979cd399e7 | 2026-09-09 | Warnings | M013 362O9ITL9D |
| dual action | ACETAMINOPHEN, IBUPROFEN | Rite Aid Corporation | 54b08d24-d5e9-4111-9d97-329896e8309d | 2026-09-09 | Warnings | 362O9ITL9D |
| Mucus Relief Cold Flu and Sore Throat Maximum Strength | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Raritan Pharmaceuticals Inc | 2cb3e17f-3858-4773-a53f-0860ae6ff1b9 | 2026-09-09 | Warnings | 362O9ITL9D |
| Lanolin, Petrolatum | LANOLIN, PETROLATUM | CVS Pharmacy, Inc. | 606f65a8-08fd-4ab6-9d68-03ddf662bdf0 | 2026-09-09 | Warnings, Adverse reactions | 4T6H12BN9U |
| Advanced Healing | PETROLATUM | Walgreen Co. | 22bd8e87-965c-466b-bb9b-7d4753e500bc | 2026-09-09 | Warnings, Adverse reactions | 4T6H12BN9U |
| polymyxin b sulfate and trimethoprim sulfate | POLYMYXIN B SULFATE AND TRIMETHOPRIM SULFATE | REMEDYREPACK INC. | c68818b2-d849-41d2-be07-731244afbbac | 2026-09-09 | Warnings, Adverse reactions | 19371312D4 |
| Magic Cream | PAIN RELIEVING OINTMENT | Jiangxi Baikang Medical Products Co., Ltd. | 5b0f2515-47e9-603f-e063-6294a90af9d4 | 2026-09-09 | Warnings | M017 |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | W Aesthetics | 5b0f2c8f-d6fa-5e25-e063-6394a90a084d | 2026-09-09 | Warnings | 15FIX9V2JP |
| North Woods Derma Foam Hand Sanitizer | BENZALKONIUM CHLORIDE | Superior Chemical Corporation | ad51a175-2b91-fd14-e053-2995a90ad54d | 2026-09-09 | Warnings | F5UM2KM3W7 |
| Alcohol Free Foaming Hand Sanitizer | BENZALKONIUM CHLORIDE | Betco Corporation, Ltd. | 7e038b0a-4813-4f4b-ad66-0584d75a064f | 2026-09-09 | Warnings | F5UM2KM3W7 |
| Burn Cream | BENZALKONIUM CHLORIDE, LIDOCAINE HCI | Trifecta Pharmaceuticals USA LLC | e9a9fc7c-31da-ea3f-e053-2a95a90a0eab | 2026-09-09 | Warnings | F5UM2KM3W7 |
| Ultra Blue Antibacterial Foaming Skin Cleanser | BENZALKONIUM CHLORIDE | Betco Corporation, Ltd | aa8f5b05-882d-d05a-e053-2995a90abaea | 2026-09-09 | Warnings | F5UM2KM3W7 |
| Burn Gel | LIDOCAINE HCI | Trifecta Pharmaceuticals USA LLC | e9d3e9be-1036-fad0-e053-2a95a90a6efe | 2026-09-09 | Warnings | M017 |
| Triple Antibiotic | BACITRACIN ZINC, NEOMYCIN SULFATE, AND POLYMYXIN B SULFATE | NuCare Pharmaceutical, Inc. | 5b14499e-e45c-7c05-e063-6294a90a1cc2 | 2026-09-09 | Warnings | 057Y626693 19371312D4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.