max tussin cough and chest congestion dm sugar free

Generic: dextromethorphan hbr, guaifenesin

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name max tussin cough and chest congestion dm sugar free
Generic Name dextromethorphan hbr, guaifenesin
Labeler atlantic biologicals corp.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/10mL, guaifenesin 200 mg/10mL

Manufacturer
ATLANTIC BIOLOGICALS CORP.

Identifiers & Regulatory

Product NDC 17856-1126
Product ID 17856-1126_34f59881-a27e-6c09-e063-6394a90a619f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M
Listing Expiration 2026-12-31
Marketing Start 2023-05-15

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178561126
Hyphenated Format 17856-1126

Supplemental Identifiers

RxCUI
996520
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name max tussin cough and chest congestion dm sugar free (source: ndc)
Generic Name dextromethorphan hbr, guaifenesin (source: ndc)
Application Number M (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/10mL
  • 200 mg/10mL
source: ndc
Packaging
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1126-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-1126-3)
  • 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1126-2) / 10 mL in 1 CUP, UNIT-DOSE (17856-1126-4)
source: ndc

Packages (2)

17856-1126-1 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1126-1) / 5 mL in 1 CUP, UNIT-DOSE (17856-1126-3) 17856-1126-2 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1126-2) / 10 mL in 1 CUP, UNIT-DOSE (17856-1126-4)

Ingredients (2)

dextromethorphan hydrobromide (20 mg/10mL) guaifenesin (200 mg/10mL)

Linked Drug Pages (1)

MAX Tussin Cough and Chest Congestion DM Sugar Free ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "34f59881-a27e-6c09-e063-6394a90a619f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["996520"], "spl_set_id": ["8f496c61-41a6-41ba-80f5-7a5309c4d18b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["ATLANTIC BIOLOGICALS CORP."]}, "finished": true, "packaging": [{"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1126-1)  / 5 mL in 1 CUP, UNIT-DOSE (17856-1126-3)", "package_ndc": "17856-1126-1", "marketing_start_date": "20241216"}, {"sample": false, "description": "72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1126-2)  / 10 mL in 1 CUP, UNIT-DOSE (17856-1126-4)", "package_ndc": "17856-1126-2", "marketing_start_date": "20241216"}], "brand_name": "MAX Tussin Cough and Chest Congestion DM Sugar Free", "product_id": "17856-1126_34f59881-a27e-6c09-e063-6394a90a619f", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "17856-1126", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "ATLANTIC BIOLOGICALS CORP.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAX Tussin Cough and Chest Congestion DM Sugar Free", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/10mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/10mL"}], "application_number": "M", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230515", "listing_expiration_date": "20261231"}