NDC 85237-1841-01 - Midol Complete
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
- 85237-1841
- Requested NDC
- 85237-1841-01
- Package NDCs from labels
- 85237-1841-1, 85237-1841-2, 85237-1841-3, 85237-1841-4, 85237-1841-5, 85237-1841-01
- Manufacturer
- Select Consumer Group
- Effective date
- 2026-07-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Midol Complete - Select Consumer Group | Select Consumer Group | 2026-07-03 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 85237-1841-1 | Midol Complete | 1 in 1 BLISTER PACK | TABLET | 1 | 2 | |
| 85237-1841-1 | Midol Complete | 2 in 1 POUCH | TABLET | 2 | 2 | |
| 85237-1841-2 | Midol Complete | 2 in 1 BLISTER PACK | TABLET | 2 | 2 | |
| 85237-1841-2 | Midol Complete | 2 in 1 POUCH | TABLET | 2 | 2 | |
| 85237-1841-3 | Midol Complete | 2 in 1 POUCH | TABLET | 2 | 2 | |
| 85237-1841-3 | Midol Complete | 20 in 1 BOX, UNIT-DOSE | TABLET | 20 | 2 | |
| 85237-1841-4 | Midol Complete | 2 in 1 POUCH | TABLET | 2 | 2 | |
| 85237-1841-4 | Midol Complete | 25 in 1 BOX, UNIT-DOSE | TABLET | 25 | 2 | |
| 85237-1841-5 | Midol Complete | 30 in 1 BOX, UNIT-DOSE | TABLET | 30 | 2 | |
| 85237-1841-5 | Midol Complete | 2 in 1 POUCH | TABLET | 2 | 2 |
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 |
|---|---|---|---|---|---|---|
| Excedrin Extra Strength Pain Reliever | ACETAMINOPHEN, ASPIRIN (NSAID), AND CAFFEINE | Haleon US Holdings LLC | 0faa3592-4d56-4645-9a0e-066e0bdfebb6 | 2024-04-05 | Warnings | 3G6A5W338E 362O9ITL9D |
| Acetaminophen | ACETAMINOPHEN TABLET EXTENDED RELEASE | Bryant Ranch Prepack | 61ea1796-b9c7-4cb9-9a36-60943f884875 | 2024-04-05 | Warnings | 362O9ITL9D |
| Butalbital, Acetaminophen, Caffeine and Codeine Phosphate | BUTALBITAL, ACETAMINOPHEN, CAFFEINE AND CODEINE PHOSPHATE | Bryant Ranch Prepack | 215e2a6f-ec32-4836-8fad-22c8b40ba1f1 | 2024-04-04 | Boxed warning, Warnings, Adverse reactions | 3G6A5W338E 362O9ITL9D |
| Pain Relief Childrens Dye Free | ACETAMINOPHEN | H E B | 3f9beeeb-5e27-4b81-a647-20e65f0e9fc9 | 2024-04-03 | Warnings | 362O9ITL9D |
| Butalbital, Acetaminophen and Caffeine | BUTALBITAL, ACETAMINOPHEN AND CAFFEINE | Bryant Ranch Prepack | e9dffed5-d615-4e63-9860-c0f6f23848a1 | 2024-04-03 | Boxed warning, Warnings, Adverse reactions | 3G6A5W338E 362O9ITL9D |
| Childrens Pain Relief | ACETAMINOPHEN | H E B | a0c0277e-50aa-4328-8f93-ab20c6176b2b | 2024-04-03 | Warnings | 362O9ITL9D |
| DAYTIME COLD AND FLU RELIEF | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND PHENYLEPHRINE HYDROCHLORIDE | Advanced Rx LLC | 38299cf3-e884-4676-8cc4-6dd64e7d023c | 2024-03-30 | Warnings | 362O9ITL9D |
| NIGHTTIME COLD AND FLU RELIEF | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, AND DOXYLAMINE SUCCINATE | Advanced Rx LLC | d1542362-19c5-4470-89e8-87d26e2ca8ed | 2024-03-30 | Warnings | 362O9ITL9D |
| Dual Action Pain Relief | DUAL ACTION PAIN RELIEF | Allegiant Health | fb4fc347-0f90-429f-9ca8-903e736f5496 | 2024-03-29 | Warnings | 362O9ITL9D |
| RV Illuminance Serum Tint Broad Spectrum 15 | FACE FOUNDATION WITH SPF | REVLON CONSUMER PR Consumer Products Corp | 132aab60-da19-7079-e063-6394a90a1d76 | 2024-03-27 | Warnings | 15FIX9V2JP |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | NuCare Pharmaceuticals,Inc. | c8d65aab-d6ae-bc69-e053-2a95a90a7b5e | 2024-03-27 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| ANTIGRIP Nighttime | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | Pharmadel LLC | 12de30fd-95b6-f16d-e063-6294a90aeba2 | 2024-03-27 | Warnings | 362O9ITL9D |
| Signature Care Migraine Relief | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Safeway | 66695667-97a3-4329-8ce0-0fffa8628951 | 2024-03-27 | Warnings | 3G6A5W338E 362O9ITL9D |
| RV Illuminance Serum Tint Broad Spectrum 15 Amber | FACE FOUNDATION WITH SPF | REVLON CONSUMER PR Consumer Products Corp | 2a0ac71c-e53a-5ff9-e063-6394a90a4807 | 2024-03-27 | Warnings | 15FIX9V2JP |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCL | Family Dollar (FAMILY WELLNESS) | 0044c53c-11dd-41a9-a5d9-622dd8b1c144 | 2024-03-27 | Warnings | 362O9ITL9D |
| EltaMD UV Pure SPF47 | ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN | CP Skin Health Group, Inc. | 9afe900b-4186-4189-a871-ad6f26fc26e4 | 2024-03-27 | Warnings | 15FIX9V2JP |
| Headache Relief Extra Strength | ACETAMINOPHEN, ASPIRIN, CAFFEINE | Family Dollar (FAMILY WELLNESS) | 650cb15e-c448-4df3-b0f8-4398be05d841 | 2024-03-27 | Warnings | 3G6A5W338E 362O9ITL9D |
| Envirotox | TRITICUM AESTIVUM, BERBERIS VULGARIS, LAPPA MAJOR, RHAMNUS PURSHIANA, SENNS (CASSIA ANGUSTIFOLIA), PHYTOLACCA DECANDRA, GLYCYRRHIZA GLABRA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, ACETONUM ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM. | BioActive Nutritional, Inc. | 2b5cfdba-cf4d-4eb0-8c60-20eac6922663 | 2024-03-26 | Warnings | 6DC9Q167V3 |
| rugby infants acetaminophen | ACETAMINOPHEN | Rugby Laboratories | 8aa9ac68-ca61-4163-a876-52034138c1ea | 2024-03-25 | Warnings | 362O9ITL9D |
| SPF 50 Mineral Based Facial Sunscreen | TITANIUM DIOXIDE, ZINC OXIDE | Hutton, Kathleen MD | 5cf0d2e3-d496-424c-ac75-70ff5b87e9ca | 2024-03-25 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.