mucus relief

Generic: guaifenesin

Labeler: nuvicare llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler nuvicare llc
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

guaifenesin 1200 mg/1

Manufacturer
NUVICARE LLC

Identifiers & Regulatory

Product NDC 84324-034
Product ID 84324-034_e4832528-9f83-4a91-9c15-e8723e045187
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA213420
Listing Expiration 2026-12-31
Marketing Start 2025-12-04

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 84324034
Hyphenated Format 84324-034

Supplemental Identifiers

RxCUI
310621
UPC
0384324000442
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 ANDA213420 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 24 TABLET, EXTENDED RELEASE in 1 BOTTLE (84324-034-01)
source: ndc

Packages (1)

84324-034-01 24 TABLET, EXTENDED RELEASE in 1 BOTTLE (84324-034-01)

Ingredients (1)

guaifenesin (1200 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": "e4832528-9f83-4a91-9c15-e8723e045187", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0384324000442"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["d6734345-29a1-4356-a063-ff37ed4fbe9a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["NUVICARE LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 TABLET, EXTENDED RELEASE in 1 BOTTLE (84324-034-01)", "package_ndc": "84324-034-01", "marketing_start_date": "20251204"}], "brand_name": "Mucus Relief", "product_id": "84324-034_e4832528-9f83-4a91-9c15-e8723e045187", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "84324-034", "generic_name": "Guaifenesin", "labeler_name": "NUVICARE LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA213420", "marketing_category": "ANDA", "marketing_start_date": "20251204", "listing_expiration_date": "20261231"}