mucus relief

Generic: guaifenesin

Labeler: dolgencorp, inc. (dollar general & rexall)
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler dolgencorp, inc. (dollar general & rexall)
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 600 mg/1

Manufacturer
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

Identifiers & Regulatory

Product NDC 55910-739
Product ID 55910-739_2f49161f-a4cf-4b5c-bc7d-dace78ee58e8
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA207342
Marketing Start 2019-03-31
Marketing End 2027-02-01

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 55910739
Hyphenated Format 55910-739

Supplemental Identifiers

RxCUI
636522
UPC
0359726731201
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
  • 20 BLISTER PACK in 1 CARTON (55910-739-20) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

55910-739-20 20 BLISTER PACK in 1 CARTON (55910-739-20) / 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": "2f49161f-a4cf-4b5c-bc7d-dace78ee58e8", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0359726731201"], "unii": ["495W7451VQ"], "rxcui": ["636522"], "spl_set_id": ["32f58b4a-3e1b-424f-8296-a9bf9a7d7025"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (55910-739-20)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55910-739-20", "marketing_end_date": "20270201", "marketing_start_date": "20190331"}], "brand_name": "Mucus Relief", "product_id": "55910-739_2f49161f-a4cf-4b5c-bc7d-dace78ee58e8", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "55910-739", "generic_name": "Guaifenesin", "labeler_name": "Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)", "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": "20270201", "marketing_start_date": "20190331"}