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 |
|---|---|---|---|---|---|---|
| Severe Cold and Flu Plus Congestion | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, GUAIFENESIN, PHENYLEPHRINE HCL | COSTCO WHOLESALE CORPORATION | 5180abbc-c6c4-4b82-b6e7-4504e3bcff0f | 2026-04-23 | Warnings | M012 |
| GUAIFENESIN AND DEXTROMETHORPHAN HBR | GUAIFENESIN AND DEXTROMETHORPHAN HBR | TOPCO ASSOCIATES LLC | 3a9737c0-e413-dfd1-e063-6294a90aaebd | 2026-04-23 | Warnings | 9D2RTI9KYH 495W7451VQ |
| Severe Cold and Flu Night time | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCL | HyVee Inc | 4f963491-e1f0-494d-acb6-5f4d2b267d4a | 2026-04-22 | Warnings | M012 9D2RTI9KYH |
| Guaifenesin and Dextromethorphan HBr | GUAIFENESIN AND DEXTROMETHORPHAN HBR | OHM LABORATORIES INC | f2eb5494-2672-444f-afa3-d1ef8ed1eaa1 | 2026-04-22 | Warnings | 9D2RTI9KYH 495W7451VQ |
| Vicks Sinex SEVERE MOISTURIZING ULTRA FINE MIST | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH | f4b01827-7444-3bfc-e053-2a95a90aebed | 2026-04-22 | Warnings | M012 |
| Vicks Sinex SEVERE ORIGINAL ULTRA FINE MIST | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH, | cfd43b8f-8064-6b88-e053-2a95a90a329e | 2026-04-22 | Warnings | M012 |
| Vicks Sinex Severe Original | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH | cfd048c9-2f33-101d-e053-2995a90ad854 | 2026-04-22 | Warnings | M012 |
| Vicks Sinex SEVERE VapoCOOL ULTRA FINE MIST | OXYMETAZOLINE HYDROCHLORIDE | Procter & Gamble Manufacturing GmbH | d0768332-7c24-7c30-e053-2a95a90a26d4 | 2026-04-22 | Warnings | M012 |
| Histanaz | PSEUDOEPHEDRINE HCL, PYRILAMINE MALEATE | Capital Pharmaceutical, LLC | 3e87d0f3-f16c-5972-e063-6294a90acc8a | 2026-04-22 | Warnings | M012 |
| Good Sense Severe Daytime Cold and Flu | ACETAMINOPHEN, DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | L. Perrigo Company | d5faf89f-3641-4be1-8d43-35504f12fe8d | 2026-04-22 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Multi-Symptom Cold childrens | DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL | WALMART INC. | 5ee5eb75-fc56-42a1-bf2c-b9c10ea8bfd4 | 2026-04-22 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| good sense nasal | OXYMETAZOLINE HYDROCHLORIDE | L. Perrigo Company | 95f23049-e523-4c59-904c-b8e9ae82602c | 2026-04-22 | Warnings | M012 |
| Pure Eyes Sterile Eyes | NAPHAZOLINE HYDROCHLORIDE AND GLYCERIN | SAMSON PHARMACEUTICAL | c0234e82-211f-4731-ac48-12db13b16e8a | 2026-04-21 | Warnings | PDC6A3C0OX |
| Dr. Carrasco Pain Relief | MENTHOL | Carrasco Enterprises, Inc. | befa8526-f468-428e-a829-422c2ea48612 | 2026-04-21 | Warnings | L7T10EIP3A |
| SOMBRA COOL THERAPY | MENTHOL | SOMBRA COSMETICS INC. | 87e9b16b-1cab-48f7-b9e4-1c3eaeeb3ca3 | 2026-04-21 | Warnings | L7T10EIP3A |
| Mucinex Childrens FreeFrom Multi-Symptom Cold and Stuffy Nose | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE | Reckitt Benckiser LLC | c07dad99-87b0-419b-9230-7c22a77ecf9e | 2026-04-21 | Warnings | M012 9D2RTI9KYH 495W7451VQ |
| Mucinex D Maximum Strength | GUAIFENESIN AND PSEUDOEPHEDRINE HYDROCHLORIDE | Reckitt Benckiser LLC | d9264518-2f2c-498f-b733-6f3397336a01 | 2026-04-21 | Warnings | 495W7451VQ |
| Cough and Cold HBP | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HBR | Valu Merchandisers Company | 83db90da-9155-4f6a-8209-44c87d14b696 | 2026-04-21 | Warnings | M012 9D2RTI9KYH |
| Pain, Headache and Cough | ACETAMINOPHEN, DEXTROMETHORPHAN HBR | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | 613a2516-fc61-4bb4-bd44-ca6004548193 | 2026-04-21 | Warnings | M012 9D2RTI9KYH |
| Guaifenesin and Dextromethorphan Hydrobromide | GUAIFENESIN AND DEXTROMETHORPHAN HYDROBROMIDE | CVS PHARMACY, INC | dd00dfc0-e523-4dec-8fc0-50363eadec57 | 2026-04-20 | Warnings | 9D2RTI9KYH 495W7451VQ |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.