mucus relief

Generic: guaifenesin

Labeler: prodose, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief
Generic Name guaifenesin
Labeler prodose, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1

Manufacturer
Prodose, Inc.

Identifiers & Regulatory

Product NDC 68210-4158
Product ID 68210-4158_49490f71-0257-e358-e063-6394a90a394a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2027-12-31
Marketing Start 2020-03-10

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 682104158
Hyphenated Format 68210-4158

Supplemental Identifiers

RxCUI
359601
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 M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
source: ndc
Packaging
  • 1 BOTTLE in 1 BOTTLE (68210-4158-1) / 15 TABLET in 1 BOTTLE
source: ndc

Packages (1)

68210-4158-1 1 BOTTLE in 1 BOTTLE (68210-4158-1) / 15 TABLET in 1 BOTTLE

Ingredients (1)

guaifenesin (400 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": "49490f71-0257-e358-e063-6394a90a394a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["359601"], "spl_set_id": ["7e5de5b0-18f0-4807-8686-da9821f918ce"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Prodose, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOTTLE (68210-4158-1)  / 15 TABLET in 1 BOTTLE", "package_ndc": "68210-4158-1", "marketing_start_date": "20210525"}], "brand_name": "MUCUS RELIEF", "product_id": "68210-4158_49490f71-0257-e358-e063-6394a90a394a", "dosage_form": "TABLET", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "68210-4158", "generic_name": "GUAIFENESIN", "labeler_name": "Prodose, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MUCUS RELIEF", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200310", "listing_expiration_date": "20271231"}