mucus relief

Generic: guaifenesin 200 mg

Labeler: richmond pharmaceuticals, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin 200 mg
Labeler richmond pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 200 mg/1

Manufacturer
Richmond Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 54738-980
Product ID 54738-980_73570295-8ab7-1c19-e053-2991aa0a6b82
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH FINAL
Application Number part341
Listing Expiration 2026-12-31
Marketing Start 2016-03-01

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 54738980
Hyphenated Format 54738-980

Supplemental Identifiers

RxCUI
197741
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 200 mg (source: ndc)
Application Number part341 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (54738-980-01)
source: ndc

Packages (1)

54738-980-01 100 TABLET in 1 BOTTLE (54738-980-01)

Ingredients (1)

guaifenesin (200 mg/1)

Linked Drug Pages (1)

Mucus Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "73570295-8ab7-1c19-e053-2991aa0a6b82", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["197741"], "spl_set_id": ["e20927a1-d402-48c1-ba00-0745ddd0a0e7"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Richmond Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54738-980-01)", "package_ndc": "54738-980-01", "marketing_start_date": "20160301"}], "brand_name": "Mucus Relief", "product_id": "54738-980_73570295-8ab7-1c19-e053-2991aa0a6b82", "dosage_form": "TABLET", "product_ndc": "54738-980", "generic_name": "Guaifenesin 200 mg", "labeler_name": "Richmond Pharmaceuticals, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "200 mg/1"}], "application_number": "part341", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20160301", "listing_expiration_date": "20261231"}