daytime severe cold and cough

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl

Labeler: h e b
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daytime severe cold and cough
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl
Labeler h e b
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/30mL, dextromethorphan hydrobromide 20 mg/30mL, phenylephrine hydrochloride 10 mg/30mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-718
Product ID 37808-718_f32e1308-7bd4-4a41-9d9b-035a0fc31833
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-03-31

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] sigma-1 agonist [epc] sigma-1 receptor agonists [moa] uncompetitive n-methyl-d-aspartate receptor antagonist [epc] uncompetitive nmda receptor antagonists [moa] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 37808718
Hyphenated Format 37808-718

Supplemental Identifiers

RxCUI
1113705
UPC
0041220762910
UNII
362O9ITL9D 9D2RTI9KYH 04JA59TNSJ

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 daytime severe cold and cough (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/30mL
  • 20 mg/30mL
  • 10 mg/30mL
source: ndc
Packaging
  • 245 mL in 1 BOTTLE, PLASTIC (37808-718-83)
source: ndc

Packages (1)

37808-718-83 245 mL in 1 BOTTLE, PLASTIC (37808-718-83)

Ingredients (3)

acetaminophen (650 mg/30mL) dextromethorphan hydrobromide (20 mg/30mL) phenylephrine hydrochloride (10 mg/30mL)

Linked Drug Pages (1)

Daytime Severe Cold and Cough ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f32e1308-7bd4-4a41-9d9b-035a0fc31833", "openfda": {"upc": ["0041220762910"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1113705"], "spl_set_id": ["9f533092-060c-4379-9a77-ecfea8aa46e1"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245 mL in 1 BOTTLE, PLASTIC (37808-718-83)", "package_ndc": "37808-718-83", "marketing_start_date": "20230331"}], "brand_name": "Daytime Severe Cold and Cough", "product_id": "37808-718_f32e1308-7bd4-4a41-9d9b-035a0fc31833", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "37808-718", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Daytime Severe Cold and Cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/30mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/30mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/30mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230331", "listing_expiration_date": "20261231"}