axiv sinus severe mucus
Generic: acetaminophen, guaifenesin, phenylephrine hydrocloride
Labeler: vivunt pharma llcDrug Facts
Product Profile
Brand Name
axiv sinus severe mucus
Generic Name
acetaminophen, guaifenesin, phenylephrine hydrocloride
Labeler
vivunt pharma llc
Dosage Form
CAPSULE, LIQUID FILLED
Routes
Active Ingredients
acetaminophen 325 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
82706-020
Product ID
82706-020_3f04ea00-9815-32e5-e063-6294a90a14c6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M012
Listing Expiration
2026-12-31
Marketing Start
2024-03-08
Pharmacologic Class
Established (EPC)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82706020
Hyphenated Format
82706-020
Supplemental Identifiers
RxCUI
UPC
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
axiv sinus severe mucus (source: ndc)
Generic Name
acetaminophen, guaifenesin, phenylephrine hydrocloride (source: ndc)
Application Number
M012 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 325 mg/1
- 200 mg/1
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (82706-020-01) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
- 50 POUCH in 1 CARTON (82706-020-03) / 2 CAPSULE, LIQUID FILLED in 1 POUCH
- 25 POUCH in 1 CARTON (82706-020-04) / 25 CAPSULE, LIQUID FILLED in 1 POUCH
Packages (3)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f04ea00-9815-32e5-e063-6294a90a14c6", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0850047780386", "0850047780607"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["2049223"], "spl_set_id": ["13245298-8b78-e177-e063-6294a90a6bec"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["VIVUNT PHARMA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (82706-020-01) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK", "package_ndc": "82706-020-01", "marketing_start_date": "20240308"}, {"sample": false, "description": "50 POUCH in 1 CARTON (82706-020-03) / 2 CAPSULE, LIQUID FILLED in 1 POUCH", "package_ndc": "82706-020-03", "marketing_start_date": "20240705"}, {"sample": false, "description": "25 POUCH in 1 CARTON (82706-020-04) / 25 CAPSULE, LIQUID FILLED in 1 POUCH", "package_ndc": "82706-020-04", "marketing_start_date": "20250212"}], "brand_name": "AXIV Sinus Severe Mucus", "product_id": "82706-020_3f04ea00-9815-32e5-e063-6294a90a14c6", "dosage_form": "CAPSULE, LIQUID FILLED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "82706-020", "generic_name": "Acetaminophen, Guaifenesin, Phenylephrine Hydrocloride", "labeler_name": "VIVUNT PHARMA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AXIV Sinus Severe Mucus", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240308", "listing_expiration_date": "20261231"}