tussin dm daytime
Generic: dextromethorphan hbr, guaifenesin
Labeler: cvs woonsocket prescription center, incorporatedDrug Facts
Product Profile
Brand Name
tussin dm daytime
Generic Name
dextromethorphan hbr, guaifenesin
Labeler
cvs woonsocket prescription center, incorporated
Dosage Form
SOLUTION
Routes
Active Ingredients
dextromethorphan hydrobromide 20 mg/20mL, guaifenesin 400 mg/20mL
Manufacturer
Identifiers & Regulatory
Product NDC
51316-304
Product ID
51316-304_8856c13d-7454-48ae-b245-afb09a4a5926
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2027-12-31
Marketing Start
2023-04-18
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
51316304
Hyphenated Format
51316-304
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
tussin dm daytime (source: ndc)
Generic Name
dextromethorphan hbr, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/20mL
- 400 mg/20mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (51316-304-19) / 237 mL in 1 BOTTLE, PLASTIC
- 1 BOTTLE, PLASTIC in 1 CARTON (51316-304-36) / 118 mL in 1 BOTTLE, PLASTIC
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8856c13d-7454-48ae-b245-afb09a4a5926", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["432d4833-2eaf-4f7c-b6b4-41043a6b7e2a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (51316-304-19) / 237 mL in 1 BOTTLE, PLASTIC", "package_ndc": "51316-304-19", "marketing_start_date": "20230418"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (51316-304-36) / 118 mL in 1 BOTTLE, PLASTIC", "package_ndc": "51316-304-36", "marketing_start_date": "20230418"}], "brand_name": "Tussin DM Daytime", "product_id": "51316-304_8856c13d-7454-48ae-b245-afb09a4a5926", "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": "51316-304", "generic_name": "Dextromethorphan HBr, Guaifenesin", "labeler_name": "CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tussin DM", "brand_name_suffix": "Daytime", "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": "20230418", "listing_expiration_date": "20271231"}