adult tussin dm
Generic: dextromethorphan hydrobromide, guaifenesin
Labeler: publix super markets incDrug Facts
Product Profile
Brand Name
adult tussin dm
Generic Name
dextromethorphan hydrobromide, guaifenesin
Labeler
publix super markets inc
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 200 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
56062-607
Product ID
56062-607_8de61363-e77f-4ee4-ad4e-542cc09942dd
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2022-07-21
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
56062607
Hyphenated Format
56062-607
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
adult tussin dm (source: ndc)
Generic Name
dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 200 mg/20mL
Packaging
- 1 BOTTLE in 1 CARTON (56062-607-26) / 118 mL in 1 BOTTLE
- 1 BOTTLE in 1 CARTON (56062-607-34) / 237 mL in 1 BOTTLE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8de61363-e77f-4ee4-ad4e-542cc09942dd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1790650"], "spl_set_id": ["25b2ad8a-5835-4496-815f-73a7fb40dcfd"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-607-26) / 118 mL in 1 BOTTLE", "package_ndc": "56062-607-26", "marketing_start_date": "20220721"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-607-34) / 237 mL in 1 BOTTLE", "package_ndc": "56062-607-34", "marketing_start_date": "20220728"}], "brand_name": "adult tussin dm", "product_id": "56062-607_8de61363-e77f-4ee4-ad4e-542cc09942dd", "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": "56062-607", "generic_name": "dextromethorphan hydrobromide, guaifenesin", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "adult tussin dm", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220721", "listing_expiration_date": "20261231"}