mucus relief

Generic: guaifenesin

Labeler: united natural foods, inc. dba unfi
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler united natural foods, inc. dba unfi
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
United Natural Foods, Inc. dba UNFI

Identifiers & Regulatory

Product NDC 41163-731
Product ID 41163-731_1cc1009f-4bb7-4eed-aa15-8dc46782d3ad
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Listing Expiration 2026-12-31
Marketing Start 2018-09-30

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 41163731
Hyphenated Format 41163-731

Supplemental Identifiers

RxCUI
636522
UPC
0041163500853
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 ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 20 BLISTER PACK in 1 CARTON (41163-731-20) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

guaifenesin (600 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1cc1009f-4bb7-4eed-aa15-8dc46782d3ad", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0041163500853"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["e7d457a6-05f9-407c-bf9b-a82e3cf2568c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (41163-731-20)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "41163-731-20", "marketing_start_date": "20180930"}], "brand_name": "Mucus Relief", "product_id": "41163-731_1cc1009f-4bb7-4eed-aa15-8dc46782d3ad", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "41163-731", "generic_name": "Guaifenesin", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "600 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_start_date": "20180930", "listing_expiration_date": "20261231"}