cold relief multi-symptom daytime

Generic: acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride

Labeler: meijer
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cold relief multi-symptom daytime
Generic Name acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
Labeler meijer
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Meijer

Identifiers & Regulatory

Product NDC 41250-138
Product ID 41250-138_2434afd9-28ec-cf6b-e063-6294a90af1a5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Marketing Start 2014-11-07
Marketing End 2026-05-31

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 41250138
Hyphenated Format 41250-138

Supplemental Identifiers

RxCUI
1094538
UPC
0708820931848
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 relief multi-symptom daytime (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 (41250-138-05) / 12 TABLET, COATED in 1 BLISTER PACK
source: ndc

Packages (1)

41250-138-05 2 BLISTER PACK in 1 CARTON (41250-138-05) / 12 TABLET, COATED in 1 BLISTER PACK

Ingredients (3)

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

Linked Drug Pages (1)

COLD RELIEF MULTI-SYMPTOM DAYTIME ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2434afd9-28ec-cf6b-e063-6294a90af1a5", "openfda": {"upc": ["0708820931848"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "04JA59TNSJ"], "rxcui": ["1094538"], "spl_set_id": ["c08d9fef-26a0-4678-aa75-193019249435"], "manufacturer_name": ["Meijer"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (41250-138-05)  / 12 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "41250-138-05", "marketing_end_date": "20260531", "marketing_start_date": "20141107"}], "brand_name": "COLD RELIEF MULTI-SYMPTOM DAYTIME", "product_id": "41250-138_2434afd9-28ec-cf6b-e063-6294a90af1a5", "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": "41250-138", "generic_name": "ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "Meijer", "product_type": "HUMAN OTC DRUG", "brand_name_base": "COLD RELIEF MULTI-SYMPTOM DAYTIME", "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_end_date": "20260531", "marketing_start_date": "20141107"}