medi-first cough cold
Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler: unifirst first aid corporationDrug Facts
Product Profile
Brand Name
medi-first cough cold
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
Labeler
unifirst first aid corporation
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, guaifenesin 100 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
47682-835
Product ID
47682-835_3e4fe7f8-b07f-5ac2-e063-6394a90afc08
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2022-09-26
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
47682835
Hyphenated Format
47682-835
Supplemental Identifiers
RxCUI
UPC
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
medi-first cough cold (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 100 mg/1
- 5 mg/1
Packaging
- 75 PACKET in 1 BOX (47682-835-36) / 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)
- 40 PACKET in 1 BOX (47682-835-80) / 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)
- 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)
Packages (3)
Ingredients (4)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e4fe7f8-b07f-5ac2-e063-6394a90afc08", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0347682483586", "0347682935801", "0347682435806"], "unii": ["9D2RTI9KYH", "362O9ITL9D", "04JA59TNSJ", "495W7451VQ"], "rxcui": ["1098435"], "spl_set_id": ["e64c283b-0efa-0bfd-e053-2a95a90ab71d"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Unifirst First Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "75 PACKET in 1 BOX (47682-835-36) / 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)", "package_ndc": "47682-835-36", "marketing_start_date": "20221212"}, {"sample": false, "description": "40 PACKET in 1 BOX (47682-835-80) / 2 TABLET, FILM COATED in 1 PACKET (47682-835-99)", "package_ndc": "47682-835-80", "marketing_start_date": "20220926"}, {"sample": false, "description": "2 TABLET, FILM COATED in 1 PACKET (47682-835-99)", "package_ndc": "47682-835-99", "marketing_start_date": "20220926"}], "brand_name": "Medi-First Cough Cold", "product_id": "47682-835_3e4fe7f8-b07f-5ac2-e063-6394a90afc08", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "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]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "47682-835", "generic_name": "Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride", "labeler_name": "Unifirst First Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Medi-First Cough Cold", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "GUAIFENESIN", "strength": "100 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220926", "listing_expiration_date": "20261231"}