cold max
Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler: marc glassman, inc.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
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68998238
Hyphenated Format
68998-238
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
cold max (source: ndc)
Generic Name
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (68998-238-05) / 12 TABLET, COATED in 1 BLISTER PACK
Packages (1)
Ingredients (3)
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"}