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
- 2026-10-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Drug Facts | ATLANTIC BIOLOGICALS CORP. | 2026-10-12 | 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 |
|---|---|---|---|---|---|---|
| LidoMedix | LIDOCAINE, MENTHOL, CAMPHOR | Absolute Therapeutics, LLC | 53d504ef-eea3-6a47-e063-6394a90a1f65 | 2026-06-09 | Warnings | L7T10EIP3A |
| Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Meijer Distribution Inc | 932b11b1-f4a0-417a-bfa1-05261a172155 | 2026-06-08 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| NO DRIP NASAL MIST | OXYMETAZOLINE HYDROCHLORIDE | Kroger Company | 957efbcf-b6d3-4793-bb6e-27e99c9be905 | 2026-06-08 | Warnings | M012 |
| DAYTIME SEVERE COLD AND FLU | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 493caecb-e687-49ea-b7a1-2a5b9376896d | 2026-06-08 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Severe Cold and Flu Relief | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | CVS PHARMACY | 4ad10fd7-c088-4356-9d34-a95cfe3a4133 | 2026-06-08 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| XIMONTH Fungi Free Bee Venom Nail Soothing Serum | GLYCERIN | Shantou Ximonth Biotechnology Co., Ltd. | 53bab969-8407-6334-e063-6294a90aa5d1 | 2026-06-08 | Warnings | 059QF0KO0R |
| Theraflu Severe Congestion Relief Nasal Mist | OXYMETAZOLINE HCL | Haleon US Holdings LLC | 4ec42064-7390-4137-a93e-57343c3c76a7 | 2026-06-08 | Warnings | M012 |
| Theraflu Severe Congestion Relief Cooling Nasal Mist | OXYMETAZOLINE HCL | Haleon US Holdings LLC | 90125a19-eed7-4ca4-a6dc-f38026c74d54 | 2026-06-08 | Warnings | M012 |
| Severe Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | Walgreen Company | 54254b61-7861-4eeb-bd3c-54fd5266f4a7 | 2026-06-08 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Guaifenesin | GUAIFENESIN | Major Pharmaceuticals | aa662428-e61f-4e22-af4d-8cf63df68c99 | 2026-06-08 | Warnings | M012 495W7451VQ |
| Chloraseptic Sore Throat Max | PHENOL AND GLYCERIN | Prestige Brands Holdings, Inc. | 882c940c-b3c3-4aa4-8d64-e4260f066ff4 | 2026-06-08 | Warnings | PDC6A3C0OX |
| Daytime Nighttime | ACETAMINOPHEN, GUAIFENESIN AND ACETAMINOPHEN, DEXTROMETHORPHAN HBR, TRIPROLIDINE HCL | TARGET CORPORATION | 47a218a0-6395-36bd-e063-6394a90a265a | 2026-06-05 | Warnings | M012 |
| Daytime Nighttime | ACETAMINOPHEN DEXTROMETHORPHAN HBR, ACETAMINOPHEN DEXTROMETHORPHAN HBR TRIPROLIDINE HCL | TARGET CORPORATION | 4779288a-9850-8490-e063-6394a90abe51 | 2026-06-05 | Warnings | M012 |
| Mucus Relief | GUAIFENESIN | NCS HealthCare of KY, LLC dba Vangard Labs | 41f4f8df-87d4-459f-af6d-3a4356a8115b | 2026-06-04 | Warnings | 495W7451VQ |
| Mucinex Fast-Max DM Max and Mucinex Fast-Max Nighttime DM Max Value Pack | DEXTROMETHORPHAN HBR, GUAIFENESIN AND TRIPROLIDINE HCL | Reckitt Benckiser LLC | 4df37cfb-299f-661f-e063-6394a90ab337 | 2026-06-04 | Warnings | M012 |
| ALKA SELTZER COLD Cold Flu Congestion Severe Fast Hot Liquid Day Night | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDE, AND DOXYLAMINE SUCCINATE | Bayer HealthCare LLC. | 53715ea4-42b3-5887-e063-6294a90a4249 | 2026-06-04 | Warnings | M012 |
| Maximum Strength Pain Relief | MENTHOL CREAM | OWELL NATURALS LLC | 5388f2c5-8cfd-a601-e063-6294a90a2e5f | 2026-06-04 | Warnings | L7T10EIP3A |
| Tussin DM | DEXTROMETHORPHAN HBR, GUAIFENESIN | Chain Drug Marketing Association, Inc. | b0d38db9-22a9-4dd8-8e0f-dd81805e724b | 2026-06-04 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Cough and Cold HBP | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | CVS PHARMACY | 65d4d7ea-c080-404e-9836-7d6bdcc5ea7d | 2026-06-04 | Warnings | M012 9D2RTI9KYH |
| Allergy Relief Childrens | DIPHENHYDRAMINE HCL | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | fe9d6a6e-38a1-44ae-a30f-596c5ec7d057 | 2026-06-03 | Warnings | M012 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.