NDC 17856-1126-01 - MAX Tussin Cough and Chest Congestion DM Sugar Free
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
- 17856-1126
- Requested NDC
- 17856-1126-01
- Package NDCs from labels
- 17856-1126-3, 17856-1126-1, 17856-1126-4, 17856-1126-2, 17856-1126-5, 17856-1126-01
- Manufacturer
- ATLANTIC BIOLOGICALS CORP.
- Effective date
- 2026-10-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | ATLANTIC BIOLOGICALS CORP. | 2026-10-23 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17856-1126-1 | MAX Tussin Cough and Chest Congestion DM Sugar Free | 72 in 1 BOX, UNIT-DOSE | LIQUID | 72 | 2 | |
| 17856-1126-2 | MAX Tussin Cough and Chest Congestion DM Sugar Free | 72 in 1 BOX, UNIT-DOSE | LIQUID | 72 | 2 | |
| 17856-1126-3 | MAX Tussin Cough and Chest Congestion DM Sugar Free | 5 mL in 1 CUP, UNIT-DOSE | LIQUID | 5 | 2 | |
| 17856-1126-4 | MAX Tussin Cough and Chest Congestion DM Sugar Free | 10 mL in 1 CUP, UNIT-DOSE | LIQUID | 10 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 17856-1126 | MAX TUSSIN COUGH AND CHEST CONGESTION DM SUGAR FREE (DEXTROMETHORPHAN HBR, GUAIFENESIN) LIQUID [ATLANTIC BIOLOGICALS CORP.] | 2 | Current NDC, 4 package rows | 20250514_8f496c61-41a6-41ba-80f5-7a5309c4d18b.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 17856-1126-1 | ML - Milliliter | 17856-1126 | 4715352a-68a3-45d7-874f-0e1c3c00f84a | 1 | 2025-05-14 |
| 17856-1126-2 | ML - Milliliter | 17856-1126 | 4da2e351-fcfd-4e8d-ad82-fa96e3ed240d | 1 | 2025-03-04 |
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 |
|---|---|---|---|---|---|---|
| Sinus Pressure and Congestion Relief PE Maximum Strength | PHENYLEPHRINE HCL | Rite Aid Corporation | fccea3c5-42af-4939-82bc-d9409b75f91f | 2026-05-01 | Warnings | M012 |
| Mucus Relief | GUAIFENESIN | Harris Teeter, LLC | f7f2e64c-0fb9-413d-80ed-4d7cc2a07e0c | 2026-05-01 | Warnings | 495W7451VQ |
| Night Time Cold and Flu original | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | Harris Teeter, LLC | cfaf4b3d-fab4-424d-adbe-aaedca58912d | 2026-04-30 | Warnings | M012 9D2RTI9KYH |
| 24 7 Relief and Recovery Pain Relieving | MENTHOL, UNSPECIFIED FORM | Triplicare Inc | 53ca807b-3ec2-4b5e-aa5a-6dcb756bb423 | 2026-04-30 | Warnings | L7T10EIP3A |
| Pain Relief Gel Roll On | MENTHOL | Trifecta Pharmaceuticals USA | 50b1a420-d5cd-6d61-e063-6294a90a0451 | 2026-04-30 | Warnings | L7T10EIP3A |
| Nighttime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE | Harris Teeter, LLC | 21e7d323-5b78-43aa-b0fc-34c2a864ab9a | 2026-04-30 | Warnings | M012 9D2RTI9KYH |
| daytime severe cold and flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | H E B | ec0b5f4b-b58c-445f-acf1-c7ce301bba64 | 2026-04-30 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Mucus Relief DM Max Maximum Strength | DEXTROMETHORPHAN HBR, GUAIFENESIN | Harris Teeter, LLC | 098428ae-e87d-4c29-8f02-1590530da58e | 2026-04-29 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Panadol Cold and Flu Day | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | Haleon US Holdings LLC | 341761b9-f0be-f816-e063-6394a90a5e63 | 2026-04-29 | Warnings | M012 9D2RTI9KYH |
| Panadol Cold and Flu Night | ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Haleon US Holdings LLC | 3417993d-8e3c-23d6-e063-6394a90a7d50 | 2026-04-29 | Warnings | M012 9D2RTI9KYH |
| Halls Sugar Free Mountain Menthol | MENTHOL | Mondelez Global LLC | 509f233e-ff01-8927-e063-6394a90a9929 | 2026-04-29 | Warnings | M012 L7T10EIP3A |
| Broncomiel Adults | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Pharmadel LLC | 509c61d3-ae16-be5c-e063-6294a90a68da | 2026-04-29 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Mucus Relief DM Max Maximum Strength | DEXTROMETHORPHAN HBR, GUAIFENESIN | TOP CARE (Topco Associates LLC) | aa1eb90c-e565-455f-8978-6f2f9e00a814 | 2026-04-29 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Tussin Cough and Chest Congestion DM adult | DEXTROMETHORPHAN HBR, GUAIFENESIN | Harris Teeter, LLC | e1280355-da81-489f-9bd2-ffea9a68010c | 2026-04-29 | Warnings | M012 996520 9D2RTI9KYH 495W7451VQ |
| Mucus Relief Childrens | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | TOPCO ASSOCIATES LLC | 7b095ec5-9951-4491-9b68-7ac0a7f10053 | 2026-04-29 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Mucus Relief Severe Congestion and Cough Maximum Strength | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | TOP CARE (Topco Associates LLC) | 98dd0ba6-0109-46b2-92df-11a030984240 | 2026-04-28 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Pain, Headache and Congestion | ACETAMINOPHEN, GUAIFENESIN | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 41a77cbb-6a4d-46a4-ab27-c7affa2cc682 | 2026-04-28 | Warnings | M012 495W7451VQ |
| Eagle Brand Medicated Roll On | MENTHOL, METHYL SALICYLATE | PT. EAGLE INDO PHARMA | 50805eee-33b3-86bd-e063-6294a90a77d8 | 2026-04-28 | Warnings | L7T10EIP3A |
| Mucus Relief | GUAIFENESIN | CVS Pharmacy | 2cfbb804-de2b-5b2f-e063-6394a90a0824 | 2026-04-28 | Warnings | 495W7451VQ |
| ALKA SELTZER COLD Cold Flu and Congestion Severe Fast Dissolve | CHLORPHENIRAMINE MALEATE, ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE, DEXTROMETHORPHAN HYDROBROMIDE | Bayer HealthCare LLC. | dd7da15a-4e0b-405f-e053-2995a90a06d2 | 2026-04-28 | Warnings | M012 9D2RTI9KYH |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.