quality choice adult tussin expectorant

Generic: guaifenesin

Labeler: quality choice (chain drug marketing association)
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name quality choice adult tussin expectorant
Generic Name guaifenesin
Labeler quality choice (chain drug marketing association)
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

guaifenesin 200 mg/10mL

Manufacturer
QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)

Identifiers & Regulatory

Product NDC 83324-332
Product ID 83324-332_3fa38f0a-8baf-42aa-e063-6394a90a594a
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2025-09-05

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 83324332
Hyphenated Format 83324-332

Supplemental Identifiers

RxCUI
310604
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 quality choice adult tussin expectorant (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/10mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (83324-332-04) / 118 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

guaifenesin (200 mg/10mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3fa38f0a-8baf-42aa-e063-6394a90a594a", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310604"], "spl_set_id": ["63dad603-fe2f-42a6-a626-5c8048a42c10"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (83324-332-04)  / 118 mL in 1 BOTTLE", "package_ndc": "83324-332-04", "marketing_start_date": "20250905"}], "brand_name": "QUALITY CHOICE ADULT TUSSIN EXPECTORANT", "product_id": "83324-332_3fa38f0a-8baf-42aa-e063-6394a90a594a", "dosage_form": "SYRUP", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "83324-332", "generic_name": "GUAIFENESIN", "labeler_name": "QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)", "product_type": "HUMAN OTC DRUG", "brand_name_base": "QUALITY CHOICE", "brand_name_suffix": "ADULT TUSSIN EXPECTORANT", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "200 mg/10mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250905", "listing_expiration_date": "20261231"}