cold terminator cold relief

Generic: phenylephrine hydrochloride, acetaminophen, dextromethorphan hydrobromide, guaifenesin

Labeler: wildman business group
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name cold terminator cold relief
Generic Name phenylephrine hydrochloride, acetaminophen, dextromethorphan hydrobromide, guaifenesin
Labeler wildman business group
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Wildman Business Group

Identifiers & Regulatory

Product NDC 84269-2556
Product ID 84269-2556_cde81c1b-0cf3-4d7b-af00-fb6a69419108
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-07-01

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 842692556
Hyphenated Format 84269-2556

Supplemental Identifiers

RxCUI
1098435
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 cold terminator cold relief (source: ndc)
Generic Name phenylephrine hydrochloride, acetaminophen, dextromethorphan hydrobromide, guaifenesin (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
  • 50 PACKET in 1 BOX (84269-2556-1) / 2 TABLET, FILM COATED in 1 PACKET
  • 75 PACKET in 1 BOX (84269-2556-2) / 2 TABLET, FILM COATED in 1 PACKET
source: ndc

Packages (2)

Ingredients (4)

acetaminophen (325 mg/1) dextromethorphan hydrobromide (10 mg/1) guaifenesin (100 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": "cde81c1b-0cf3-4d7b-af00-fb6a69419108", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "9D2RTI9KYH", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1098435"], "spl_set_id": ["e8538d9c-f9ba-40b1-b60f-f57921f39b64"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Wildman Business Group"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 PACKET in 1 BOX (84269-2556-1)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "84269-2556-1", "marketing_start_date": "20240701"}, {"sample": false, "description": "75 PACKET in 1 BOX (84269-2556-2)  / 2 TABLET, FILM COATED in 1 PACKET", "package_ndc": "84269-2556-2", "marketing_start_date": "20240701"}], "brand_name": "Cold Terminator Cold Relief", "product_id": "84269-2556_cde81c1b-0cf3-4d7b-af00-fb6a69419108", "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": "84269-2556", "generic_name": "PHENYLEPHRINE HYDROCHLORIDE, ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN", "labeler_name": "Wildman Business Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Cold Terminator", "brand_name_suffix": "Cold Relief", "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": "20240701", "listing_expiration_date": "20261231"}