Mucus Relief Maximum Strength

Generic: Guaifenesin

Labeler: Rite Aid Corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name Mucus Relief Maximum Strength
Generic Name Guaifenesin
Labeler Rite Aid Corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

GUAIFENESIN 1200 mg/1

Identifiers & Regulatory

Product NDC 11822-0732
Product ID 11822-0732_b279a2d1-7941-4862-8f85-d098ded81b05
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Marketing Start 2019-05-31
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118220732
Hyphenated Format 11822-0732

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 Maximum Strength (source: ndc)
Generic Name Guaifenesin (source: ndc)
Application Number ANDA207342 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1200 mg/1
source: ndc
Packaging
  • 42 BLISTER PACK in 1 CARTON (11822-0732-6) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

11822-0732-6 42 BLISTER PACK in 1 CARTON (11822-0732-6) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

GUAIFENESIN (1200 mg/1)

Linked Drug Pages (1)

Mucus Relief Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b279a2d1-7941-4862-8f85-d098ded81b05", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0011822739030"], "unii": ["495W7451VQ"], "rxcui": ["310621"], "spl_set_id": ["73184b46-7345-45ed-bac7-b15d5473dba9"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "42 BLISTER PACK in 1 CARTON (11822-0732-6)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11822-0732-6", "marketing_end_date": "20260228", "marketing_start_date": "20190531"}], "brand_name": "Mucus Relief Maximum Strength", "product_id": "11822-0732_b279a2d1-7941-4862-8f85-d098ded81b05", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "11822-0732", "generic_name": "Guaifenesin", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "1200 mg/1"}], "application_number": "ANDA207342", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20190531"}