mucus relief

Generic: guaifenesin

Labeler: healthlife of usa llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler healthlife of usa llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1

Manufacturer
HealthLife of USA LLC

Identifiers & Regulatory

Product NDC 69517-005
Product ID 69517-005_3fb098bb-932b-3247-e063-6294a90a26d5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-09-26

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 69517005
Hyphenated Format 69517-005

Supplemental Identifiers

RxCUI
359601
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 (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 (69517-005-02)
  • 300 TABLET in 1 BOTTLE (69517-005-03)
  • 60 TABLET in 1 BOTTLE (69517-005-60)
source: ndc

Packages (3)

Ingredients (1)

guaifenesin (400 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fb098bb-932b-3247-e063-6294a90a26d5", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["1be2a8b4-b010-4ad3-aa23-c8e4909681c8"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["HealthLife of USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "200 TABLET in 1 BOTTLE (69517-005-02)", "package_ndc": "69517-005-02", "marketing_start_date": "20250926"}, {"sample": false, "description": "300 TABLET in 1 BOTTLE (69517-005-03)", "package_ndc": "69517-005-03", "marketing_start_date": "20250926"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (69517-005-60)", "package_ndc": "69517-005-60", "marketing_start_date": "20250926"}], "brand_name": "Mucus Relief", "product_id": "69517-005_3fb098bb-932b-3247-e063-6294a90a26d5", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "69517-005", "generic_name": "Guaifenesin", "labeler_name": "HealthLife of USA LLC", "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": "20250926", "listing_expiration_date": "20261231"}