mucus relief

Generic: guaifenesin 400 mg

Labeler: cabinet health, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin 400 mg
Labeler cabinet health, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1

Manufacturer
Cabinet Health, Inc.

Identifiers & Regulatory

Product NDC 82725-1012
Product ID 82725-1012_395687f6-95e4-578c-e063-6394a90a1e6a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2024-11-01

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 827251012
Hyphenated Format 82725-1012

Supplemental Identifiers

RxCUI
359601
UPC
0691036647170
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 mucus relief (source: ndc)
Generic Name guaifenesin 400 mg (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 200 TABLET in 1 BOTTLE (82725-1012-1)
source: ndc

Packages (1)

Ingredients (1)

guaifenesin (400 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "395687f6-95e4-578c-e063-6394a90a1e6a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0691036647170"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["26a51b0e-039c-663c-e063-6394a90ad384"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cabinet Health, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (82725-1012-1)", "package_ndc": "82725-1012-1", "marketing_start_date": "20241101"}], "brand_name": "Mucus Relief", "product_id": "82725-1012_395687f6-95e4-578c-e063-6394a90a1e6a", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "82725-1012", "generic_name": "Guaifenesin 400 mg", "labeler_name": "Cabinet Health, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241101", "listing_expiration_date": "20261231"}