severe cold and cough relief daytime
Generic: acetaminohpen, dextromethorphan hbr, phenylephrine hcl
Labeler: dolgencorp, inc. (dollar general & rexall)Drug Facts
Product Profile
Brand Name
severe cold and cough relief daytime
Generic Name
acetaminohpen, dextromethorphan hbr, phenylephrine hcl
Labeler
dolgencorp, inc. (dollar general & rexall)
Dosage Form
LIQUID
Routes
Active Ingredients
acetaminophen 650 mg/30mL, dextromethorphan hydrobromide 20 mg/30mL, phenylephrine hydrochloride 10 mg/30mL
Manufacturer
Identifiers & Regulatory
Product NDC
55910-801
Product ID
55910-801_7a255665-dad4-4e8d-b7e8-52eeab203fea
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2017-03-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910801
Hyphenated Format
55910-801
Supplemental Identifiers
RxCUI
UPC
UNII
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
severe cold and cough relief daytime (source: ndc)
Generic Name
acetaminohpen, dextromethorphan hbr, phenylephrine hcl (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 650 mg/30mL
- 20 mg/30mL
- 10 mg/30mL
Packaging
- 245 mL in 1 BOTTLE, PLASTIC (55910-801-08)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7a255665-dad4-4e8d-b7e8-52eeab203fea", "openfda": {"upc": ["0349580501089"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1113705"], "spl_set_id": ["553d01a9-e8ad-4797-b55b-32f134f08af9"], "manufacturer_name": ["Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "245 mL in 1 BOTTLE, PLASTIC (55910-801-08)", "package_ndc": "55910-801-08", "marketing_start_date": "20170331"}], "brand_name": "Severe Cold and Cough Relief Daytime", "product_id": "55910-801_7a255665-dad4-4e8d-b7e8-52eeab203fea", "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": "55910-801", "generic_name": "ACETAMINOHPEN, DEXTROMETHORPHAN HBr, PHENYLEPHRINE HCL", "labeler_name": "Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Severe Cold and Cough Relief", "brand_name_suffix": "Daytime", "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": "20170331", "listing_expiration_date": "20261231"}