cold terminator cold relief
Generic: phenylephrine hydrochloride, acetaminophen, dextromethorphan hydrobromide, guaifenesin
Labeler: wildman business groupDrug 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
Active Ingredients
acetaminophen 325 mg/1, dextromethorphan hydrobromide 10 mg/1, guaifenesin 100 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
842692556
Hyphenated Format
84269-2556
Supplemental Identifiers
RxCUI
UNII
NUI
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 terminator cold relief (source: ndc)
Generic Name
phenylephrine hydrochloride, acetaminophen, dextromethorphan hydrobromide, guaifenesin (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 10 mg/1
- 100 mg/1
- 5 mg/1
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
Packages (2)
Ingredients (4)
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"}