NDC 11673-541 - daytime severe cold and cough and nighttime severe cold and cough
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
- 11673-541
- Package NDCs from labels
- 11673-541-06
- Manufacturer
- Target Corporation
- Effective date
- 2018-01-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| daytime severe cold and cough - Target Corporation | Target Corporation | 2018-01-18 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 11673-541-06 | daytime severe cold and cough and nighttime severe cold and cough | 6 in 1 CARTON | POWDER, FOR SOLUTION | 6 | 650 mg | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 11673-541 | DAYTIME SEVERE COLD AND COUGH AND NIGHTTIME SEVERE COLD AND COUGH (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL) KIT [TARGET CORPORATION] | 1 | Unmatched | 20180123_62eec235-431f-4429-b173-d4a9b45a4e36.zip |
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 |
|---|---|---|---|---|---|---|
| Large Ring Combination 9302 | LARGE RING COMBINATION | Professional Complementary Health Formulas | cced8a69-7bc0-42ad-b80a-58fc603bf765 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Domestic Animals Nosode Combination 9407 | DOMESTIC ANIMALS NOSODE COMBINATION | Professional Complementary Health Formulas | 222c28aa-e07b-4706-9fb5-585b190f1c5b | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
| Thompson Cough and Cold Multi-Symptom Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE, GUAIFENESIN, , | Thompson | e77725b1-15da-35bd-e053-2a95a90ad6ba | 2026-01-08 | Warnings | 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| Thompson Cramp Relief | ACETAMINOPHEN, PAMABROM, PYRILAMINE MALEATE | Thompson Safety | e82f607d-05b1-2c50-e053-2995a90a607e | 2026-01-08 | Warnings | 362O9ITL9D |
| Mucosan Childrens Multi-Symptom Grape | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 266c8cce-cdf9-557d-e063-6394a90a9bc3 | 2026-01-08 | Warnings | 9D2RTI9KYH 04JA59TNSJ |
| Mucosan Multi-Symptom Honey | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Menper Distributors, Inc. | 2669c620-ab70-abaa-e063-6394a90a58e7 | 2026-01-08 | Warnings | 9D2RTI9KYH 04JA59TNSJ |
| Mucosan Multi-Symptom Cherry | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 26b8c06d-4a72-3979-e063-6394a90a96d7 | 2026-01-08 | Warnings | 9D2RTI9KYH 04JA59TNSJ |
| Mucosan Max with Acetaminophen | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN AND PHENYLEPHRINE HYDROCHLORIDE | Menper Distributors, Inc. | 26a4861b-5d8e-9ec6-e063-6394a90af577 | 2026-01-08 | Warnings | 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| Mucosan Severe Multi-Symptom | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Menper Distributors, Inc. | 26a69342-f65f-cb46-e063-6394a90ade10 | 2026-01-08 | Warnings | 9D2RTI9KYH 04JA59TNSJ |
| Alka-Seltzer Plus Severe Cold PowerFast Fizz Non Drowsy | ASPRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE | Bayer HealthCare LLC. | a355d987-77ce-9e32-e053-2995a90a6431 | 2026-01-08 | Warnings | 9D2RTI9KYH |
| 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 | 9D2RTI9KYH 04JA59TNSJ 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 | 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| Alka-Seltzer Plus Severe Cold Night PowerFast Fizz | ASPIRIN, DOXYLAMINE SUCCINATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE | Bayer HealthCare LLC. | c1fae6c7-bbac-1320-e053-2a95a90aac5a | 2026-01-08 | Warnings | 9D2RTI9KYH |
| 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 | 9D2RTI9KYH 04JA59TNSJ 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 | 9D2RTI9KYH 04JA59TNSJ 362O9ITL9D |
| VANACOF XP Cough / Chest Congestion | DEXTROMETHORPHAN HBR, GUAIFENESIN | GM Pharmaceuticals, INC | 0b3a8cc1-a49f-e1e5-e063-6394a90a1c06 | 2026-01-08 | Warnings | 9D2RTI9KYH |
| Hydrocodone Bitartrate and Acetaminophen | HYDROCODONE BITARTRATE AND ACETAMINOPHEN | AvPAK | 678f3d54-3b62-c9e8-2ff3-a2a6bd9ecfc3 | 2026-01-08 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
| Diphenhydramine HCl | DIPHENHYDRAMINE HCL | INVAHEALTH INC | e4e4004f-77e3-569d-e053-2a95a90a73fe | 2026-01-08 | Warnings | TC2D6JAD40 |
| Preparation H Rapid Relief | GLYCERIN, LIDOCAINE, PHENYLEPHRINE HYDROCHLORIDE | Haleon US Holdings LLC | 49a93cfc-4ccd-4ef3-928f-901b9926f794 | 2026-01-08 | Warnings | 04JA59TNSJ |
| Butalbital, Acetaminophen, Caffeine | BUTALBITAL, ACETAMINOPHEN, AND CAFFEINE | Advanced Rx of Tennessee, LLC | 4871c36f-229b-4c12-e063-6394a90a028e | 2026-01-08 | Boxed warning, Warnings, Adverse reactions | 362O9ITL9D |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.