max tussin mucus and chest congestion

Generic: guaifenesin

Labeler: akron pharma inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name max tussin mucus and chest congestion
Generic Name guaifenesin
Labeler akron pharma inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

guaifenesin 200 mg/10mL

Manufacturer
Akron Pharma Inc.

Identifiers & Regulatory

Product NDC 71399-0054
Product ID 71399-0054_422cdba2-dbee-37d5-e063-6294a90ac401
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-11-03

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 713990054
Hyphenated Format 71399-0054

Supplemental Identifiers

RxCUI
310604
UPC
0371399005489
UNII
495W7451VQ
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 max tussin mucus and chest congestion (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/10mL
source: ndc
Packaging
  • 1 BOTTLE in 1 PACKAGE (71399-0054-4) / 118 mL in 1 BOTTLE
  • 473 mL in 1 BOTTLE (71399-0054-6)
  • 1 BOTTLE in 1 PACKAGE (71399-0054-8) / 236 mL in 1 BOTTLE
source: ndc

Packages (3)

71399-0054-4 1 BOTTLE in 1 PACKAGE (71399-0054-4) / 118 mL in 1 BOTTLE 71399-0054-6 473 mL in 1 BOTTLE (71399-0054-6) 71399-0054-8 1 BOTTLE in 1 PACKAGE (71399-0054-8) / 236 mL in 1 BOTTLE

Ingredients (1)

guaifenesin (200 mg/10mL)

Linked Drug Pages (1)

MAX Tussin Mucus and Chest Congestion ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "422cdba2-dbee-37d5-e063-6294a90ac401", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0371399005489"], "unii": ["495W7451VQ"], "rxcui": ["310604"], "spl_set_id": ["ac874a31-5556-4669-937f-dcb52aaecd8a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Akron Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 PACKAGE (71399-0054-4)  / 118 mL in 1 BOTTLE", "package_ndc": "71399-0054-4", "marketing_start_date": "20231103"}, {"sample": false, "description": "473 mL in 1 BOTTLE (71399-0054-6)", "package_ndc": "71399-0054-6", "marketing_start_date": "20231103"}, {"sample": false, "description": "1 BOTTLE in 1 PACKAGE (71399-0054-8)  / 236 mL in 1 BOTTLE", "package_ndc": "71399-0054-8", "marketing_start_date": "20231103"}], "brand_name": "MAX Tussin Mucus and Chest Congestion", "product_id": "71399-0054_422cdba2-dbee-37d5-e063-6294a90ac401", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "71399-0054", "generic_name": "Guaifenesin", "labeler_name": "Akron Pharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MAX Tussin Mucus and Chest Congestion", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "200 mg/10mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231103", "listing_expiration_date": "20261231"}