NDC 70518-4184-01 - Acetaminophen
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
- 70518-4184
- Requested NDC
- 70518-4184-01
- Package NDCs from labels
- 70518-4184-1, 70518-4184-0, 70518-4184-3, 70518-4184-2, 70518-4184-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-08-28
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Acetaminophen - REMEDYREPACK INC. | REMEDYREPACK INC. | 2026-08-28 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-4184-0 | Acetaminophen | 24 in 1 CARTON | INJECTION, SOLUTION | 24 | 3 | |
| 70518-4184-1 | Acetaminophen | 100 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 100 | 3 | |
| 70518-4184-2 | Acetaminophen | 25 in 1 CARTON | INJECTION, SOLUTION | 25 | 3 | |
| 70518-4184-3 | Acetaminophen | 100 mL in 1 VIAL, SINGLE-DOSE | INJECTION, SOLUTION | 100 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-4184 | ACETAMINOPHEN INJECTION, SOLUTION [REMEDYREPACK INC.] | 2 | Current NDC, 4 package rows | 20241003_464e404a-1957-44a2-a53a-f2a9d3c15bde.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70518-4184-2 | ML - Milliliter | 70518-4184 | 6e544e9d-b1e8-47d9-b918-09c72082d50a | 1 | 2026-03-17 |
| 70518-4184-3 | ML - Milliliter | 70518-4184 | 5606a6e5-2376-4b3b-885d-8fde9049149c | 1 | 2026-03-17 |
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 |
|---|---|---|---|---|---|---|
| Nighttime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE | BETTER LIVING BRANDS LLC. | 41f4bf6d-f83c-92e4-e063-6394a90aebab | 2026-01-13 | Warnings | 362O9ITL9D |
| Severe Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | HYVEE INC | 462cbf3d-51b1-dab9-e063-6394a90a70ba | 2026-01-13 | Warnings | 362O9ITL9D |
| Pain Terminator Extra Strength Pain Relief | CAFFEINE, ACETAMINOPHEN, ASPIRIN | Wildman Business Group | 8ffb02d9-92df-4d2f-a367-1c71490807fb | 2026-01-12 | Warnings | 362O9ITL9D |
| Acetaminophen and Ibuprofen | ACETAMINOPHEN AND IBUPROFEN | BIONPHARMA INC. | 4834aa7f-cb0c-ec58-e063-6394a90ae2fc | 2026-01-12 | Warnings | 362O9ITL9D |
| Tramadol Hydrochloride and Acetaminophen | TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN | AvPAK | 244f6e5d-e1b4-ba8b-ca6f-af2d8a31d5f0 | 2026-01-12 | Warnings, Adverse reactions | 362O9ITL9D |
| OXYCODONE AND ACETAMINOPHEN | OXYCODONE AND ACETAMINOPHEN | KVK-Tech, Inc. | 9986aa04-c976-4654-8ad7-b97d2eecea93 | 2026-01-12 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN | PD-Rx Pharmaceuticals, Inc. | 64696f65-415e-4ce1-a5b3-70662fbcb002 | 2026-01-12 | Warnings | 362O9ITL9D |
| Tension Headache | ACETAMINOPHEN, CAFFEINE | Cardinal Health 110, LLC. DBA Leader | 96684e3f-a13e-49c3-b437-d2627e528a2d | 2026-01-12 | Warnings | 362O9ITL9D |
| Sinu-Phen Plus Sinus Pain and Pressure | ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE | Wildman Business Group | c66e0b52-5531-4a84-ae90-8a26d27df1ec | 2026-01-12 | Warnings | 362O9ITL9D |
| Daytime Cold and Flu | DAYTIME COLD AND FLU | Allegiant Health | 69ed2da0-16b2-49eb-91b4-cc5cf328c817 | 2026-01-09 | Warnings | 362O9ITL9D |
| Butalbital, Acetaminophen, Caffeine, and Codeine Phosphate | BUTALBITAL, ACETAMINOPHEN, CAFFEINE, AND CODEINE PHOSPHATE | Actavis Pharma, Inc. | a58819b8-a52c-44a7-9ab0-c74480d98506 | 2026-01-09 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Xpect Acetaminophen | ACETAMINOPHEN | Cintas Corporation | f4aed854-730e-493d-b523-122156e08dde | 2026-01-09 | Warnings | 362O9ITL9D |
| Endotoxin Terrain Drops 2143 | ENDOTOXIN TERRAIN DROPS | Professional Complementary Health Formulas | 58842566-005a-48b5-973d-20cde2fbd701 | 2026-01-08 | Warnings | QTT17582CB |
| Thompson Cough and Cold Multi-Symptom Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE, GUAIFENESIN, , | Thompson | e77725b1-15da-35bd-e053-2a95a90ad6ba | 2026-01-08 | Warnings | 362O9ITL9D |
| Thompson Cramp Relief | ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE | Thompson Safety | e82f607d-05b1-2c50-e053-2995a90a607e | 2026-01-08 | Warnings | 362O9ITL9D |
| Mucosan Max with Acetaminophen | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 26a4861b-5d8e-9ec6-e063-6394a90af577 | 2026-01-08 | Warnings | 362O9ITL9D |
| Alka-Seltzer Plus Maximum Strength Sinus, Congestion and Pain Power Max Gels | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE , PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | e07931fc-f753-1aeb-e053-2a95a90ada3f | 2026-01-08 | Warnings | 362O9ITL9D |
| Alka Seltzer Plus Maximum Strength Sinus, Allergy And Cough Power Max Gels | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE , DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | e17eb929-209d-a2d1-e053-2a95a90a4cf3 | 2026-01-08 | Warnings | 362O9ITL9D |
| Alka-Seltzer Plus Night Severe Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, AND PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | f4c60ca1-ba59-4a92-84a5-6ba65faa56ab | 2026-01-08 | Warnings | 362O9ITL9D |
| Alka-Seltzer Plus Day Severe Cold Plus Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Bayer HealthCare LLC. | cec51eab-cce3-4965-a14e-a46d953050c4 | 2026-01-08 | Warnings | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.