maximum strength cold tabs

Generic: acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride

Labeler: jhk dba american safety & first aid
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name maximum strength cold tabs
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Labeler jhk dba american safety & first aid
Dosage Form CAPSULE, COATED
Routes
ORAL
Active Ingredients

acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, guaifenesin 100 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
JHK DBA American Safety & First Aid

Identifiers & Regulatory

Product NDC 73598-1342
Product ID 73598-1342_cf30ce4e-309a-4869-b469-ebfa2d28b80f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-06-26

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 735981342
Hyphenated Format 73598-1342

Supplemental Identifiers

UNII
362O9ITL9D 9D2RTI9KYH 495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

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 maximum strength cold tabs (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 100 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 40 PACKET in 1 BOX (73598-1342-1) / 2 CAPSULE, COATED in 1 PACKET
source: ndc

Packages (1)

73598-1342-1 40 PACKET in 1 BOX (73598-1342-1) / 2 CAPSULE, COATED in 1 PACKET

Ingredients (4)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) guaifenesin (100 mg/1) phenylephrine hydrochloride (5 mg/1)

Linked Drug Pages (1)

Maximum Strength Cold Tabs ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf30ce4e-309a-4869-b469-ebfa2d28b80f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "spl_set_id": ["e7d4fe9a-eb09-4266-90c9-290f61ce6ad0"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["JHK DBA American Safety & First Aid"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 PACKET in 1 BOX (73598-1342-1)  / 2 CAPSULE, COATED in 1 PACKET", "package_ndc": "73598-1342-1", "marketing_start_date": "20240626"}], "brand_name": "Maximum Strength Cold Tabs", "product_id": "73598-1342_cf30ce4e-309a-4869-b469-ebfa2d28b80f", "dosage_form": "CAPSULE, 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": "73598-1342", "generic_name": "acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride", "labeler_name": "JHK DBA American Safety & First Aid", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Maximum Strength Cold Tabs", "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": "20240626", "listing_expiration_date": "20261231"}