mucus relief

Generic: guaifenesin

Labeler: pioneer life sciences, llc
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

guaifenesin 1200 mg/1

Manufacturer
Pioneer Life Sciences, LLC

Identifiers & Regulatory

Product NDC 72090-012
Product ID 72090-012_022e6fd9-1e64-4364-a117-67354fed2fa0
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 72090012
Hyphenated Format 72090-012

Supplemental Identifiers

RxCUI
310621
UPC
0372090002906 0372090002913
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
  • 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-01)
  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-02)
  • 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-03)
source: ndc

Packages (3)

72090-012-01 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-01) 72090-012-02 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-02) 72090-012-03 50 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-03)

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": "022e6fd9-1e64-4364-a117-67354fed2fa0", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0372090002906", "0372090002913"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["d635b228-a51f-42d9-885c-3cd566fd352b"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Pioneer Life Sciences, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-01)", "package_ndc": "72090-012-01", "marketing_start_date": "20251204"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-02)", "package_ndc": "72090-012-02", "marketing_start_date": "20251204"}, {"sample": false, "description": "50 TABLET, EXTENDED RELEASE in 1 BOTTLE (72090-012-03)", "package_ndc": "72090-012-03", "marketing_start_date": "20251204"}], "brand_name": "Mucus Relief", "product_id": "72090-012_022e6fd9-1e64-4364-a117-67354fed2fa0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "72090-012", "generic_name": "Guaifenesin", "labeler_name": "Pioneer Life Sciences, 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"}