axiv sinus severe mucus

Generic: acetaminophen, guaifenesin, phenylephrine hydrocloride

Labeler: vivunt pharma llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug 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
ORAL
Active Ingredients

acetaminophen 325 mg/1, guaifenesin 200 mg/1, phenylephrine hydrochloride 5 mg/1

Manufacturer
VIVUNT PHARMA LLC

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)
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 82706020
Hyphenated Format 82706-020

Supplemental Identifiers

RxCUI
2049223
UPC
0850047780386 0850047780607
UNII
362O9ITL9D 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 axiv sinus severe mucus (source: ndc)
Generic Name acetaminophen, guaifenesin, phenylephrine hydrocloride (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 325 mg/1
  • 200 mg/1
  • 5 mg/1
source: ndc
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
source: ndc

Packages (3)

Ingredients (3)

acetaminophen (325 mg/1) guaifenesin (200 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": "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"}