tussin dm max

Generic: dextromethorphan hydrobromide, guaifenesin

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name tussin dm max
Generic Name dextromethorphan hydrobromide, guaifenesin
Labeler walgreen company
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-1144
Product ID 0363-1144_6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-05-24

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 03631144
Hyphenated Format 0363-1144

Supplemental Identifiers

RxCUI
1020138
UNII
9D2RTI9KYH 495W7451VQ
NUI
N0000193956 N0000008867 N0000009560

Packaging Origin

Original Packager
true

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 tussin dm max (source: ndc)
Generic Name dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/20mL
  • 400 mg/20mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (0363-1144-26) / 118 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (0363-1144-34) / 237 mL in 1 BOTTLE
source: ndc

Packages (2)

0363-1144-26 1 BOTTLE in 1 CARTON (0363-1144-26) / 118 mL in 1 BOTTLE 0363-1144-34 1 BOTTLE in 1 CARTON (0363-1144-34) / 237 mL in 1 BOTTLE

Ingredients (2)

dextromethorphan hydrobromide (20 mg/20mL) guaifenesin (400 mg/20mL)

Linked Drug Pages (1)

tussin dm max ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["756794b0-8d3b-4732-947c-a407caf400e2"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1144-26)  / 118 mL in 1 BOTTLE", "package_ndc": "0363-1144-26", "marketing_start_date": "20220524"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-1144-34)  / 237 mL in 1 BOTTLE", "package_ndc": "0363-1144-34", "marketing_start_date": "20220524"}], "brand_name": "tussin dm max", "product_id": "0363-1144_6dca6e0b-1e4e-4d4a-b085-7ae9a0c7fe8a", "dosage_form": "SOLUTION", "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": "0363-1144", "generic_name": "Dextromethorphan Hydrobromide, Guaifenesin", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "tussin dm max", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "400 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220524", "listing_expiration_date": "20261231"}