mucus relief

Generic: guaifenesin

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler rite aid corporation
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-3252
Product ID 11822-3252_0fefb6bf-bc40-4f9e-a573-2dd50356fc38
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Marketing Start 2021-09-24
Marketing End 2026-12-30

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 118223252
Hyphenated Format 11822-3252

Supplemental Identifiers

RxCUI
636522
UPC
0011822325271
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
  • 40 BLISTER PACK in 1 CARTON (11822-3252-7) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

11822-3252-7 40 BLISTER PACK in 1 CARTON (11822-3252-7) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

guaifenesin (600 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": "0fefb6bf-bc40-4f9e-a573-2dd50356fc38", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0011822325271"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["73fb2194-a582-4d3c-bc82-c5f110efcd81"], "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": "40 BLISTER PACK in 1 CARTON (11822-3252-7)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "11822-3252-7", "marketing_end_date": "20261230", "marketing_start_date": "20210924"}], "brand_name": "Mucus Relief", "product_id": "11822-3252_0fefb6bf-bc40-4f9e-a573-2dd50356fc38", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "11822-3252", "generic_name": "Guaifenesin", "labeler_name": "Rite Aid Corporation", "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_end_date": "20261230", "marketing_start_date": "20210924"}