cold max

Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride

Labeler: marc glassman, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cold max
Generic Name acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler marc glassman, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
MARC GLASSMAN, INC.

Identifiers & Regulatory

Product NDC 68998-238
Product ID 68998-238_25271acf-b60a-c1ec-e063-6294a90a6d2d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-10-05

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 68998238
Hyphenated Format 68998-238

Supplemental Identifiers

RxCUI
1094538
UPC
0094442601086
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 cold max (source: ndc)
Generic Name acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 10 mg/1
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (68998-238-05) / 12 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (3)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25271acf-b60a-c1ec-e063-6294a90a6d2d", "openfda": {"upc": ["0094442601086"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1094538"], "spl_set_id": ["e2346d0c-75cf-974c-e053-2a95a90a2857"], "manufacturer_name": ["MARC GLASSMAN, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (68998-238-05)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "68998-238-05", "marketing_start_date": "20221005"}], "brand_name": "Cold Max", "product_id": "68998-238_25271acf-b60a-c1ec-e063-6294a90a6d2d", "dosage_form": "TABLET, COATED", "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": "68998-238", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "MARC GLASSMAN, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Max", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "10 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221005", "listing_expiration_date": "20261231"}