guaifenesin

Generic: guaifenesin

Labeler: kesin pharma corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name guaifenesin
Generic Name guaifenesin
Labeler kesin pharma corporation
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

guaifenesin 100 mg/5mL

Manufacturer
KESIN PHARMA CORPORATION

Identifiers & Regulatory

Product NDC 81033-102
Product ID 81033-102_316ac9e6-8d03-f55a-e063-6294a90a8540
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2023-11-20

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 81033102
Hyphenated Format 81033-102

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 guaifenesin (source: ndc)
Generic Name guaifenesin (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/5mL
source: ndc
Packaging
  • 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-51) / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05)
  • 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10)
source: ndc

Packages (2)

81033-102-51 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-51) / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05) 81033-102-52 50 CUP, UNIT-DOSE in 1 CARTON (81033-102-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10)

Ingredients (1)

guaifenesin (100 mg/5mL)

Linked Drug Pages (2)

Guaifenesin ndc-match (0.9) Guaifenesin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "316ac9e6-8d03-f55a-e063-6294a90a8540", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ"], "rxcui": ["310604"], "spl_set_id": ["365c01b7-a197-4876-85fc-42204f787e3a"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["KESIN PHARMA CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CARTON (81033-102-51)  / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05)", "package_ndc": "81033-102-51", "marketing_start_date": "20231120"}, {"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CARTON (81033-102-52)  / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10)", "package_ndc": "81033-102-52", "marketing_start_date": "20231120"}], "brand_name": "Guaifenesin", "product_id": "81033-102_316ac9e6-8d03-f55a-e063-6294a90a8540", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]"], "product_ndc": "81033-102", "generic_name": "Guaifenesin", "labeler_name": "KESIN PHARMA CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Guaifenesin", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231120", "listing_expiration_date": "20261231"}