FDA.reportPublic FDA data

Guaifenesin

Product NDC
81033-102
11-digit product format
810330102
Labeler code
81033
Product ID
81033-102_316ac9e6-8d03-f55a-e063-6294a90a8540
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin
Dosage form
LIQUID
Route
ORAL
Labeler
KESIN PHARMA CORPORATION
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2023-11-20
Substance
GUAIFENESIN
Active strength
100 mg/5mL
Pharmacologic classes
Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
Guaifenesin
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
GUAIFENESIN100 mg/5mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
495W7451VQInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
310604Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
365c01b7-a197-4876-85fc-42204f787e3aAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81033-102-05Guaifenesin5 mL in 1 CUP, UNIT-DOSELIQUID57
81033-102-10Guaifenesin10 mL in 1 CUP, UNIT-DOSELIQUID107
81033-102-51Guaifenesin50 in 1 CARTONLIQUID507
81033-102-52Guaifenesin50 in 1 CARTONLIQUID507
81033-102-16Guaifenesin473 mL in 1 BOTTLELIQUID4731

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
81033-102-05ML - Milliliter81033-102c04493a2-a5df-4be5-86e1-38cd698bbd6312024-03-12
81033-102-10ML - Milliliter81033-102a990cc84-2678-4699-8dca-ec8808a024a412024-04-05
81033-102-16ML - Milliliter81033-1027a1f8916-cb71-4e4c-a447-b4f532f27ea312025-06-13
81033-102-51ML - Milliliter81033-102118824ef-231f-4404-85a9-9e31242703de12024-01-04
81033-102-52ML - Milliliter81033-1020be6c67c-993a-4d6d-9ecc-515e876c5d3912024-01-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81033-102GUAIFENESIN LIQUID [KESIN PHARMA CORPORATION]7Current NDC, 4 package rows20250331_365c01b7-a197-4876-85fc-42204f787e3a.zip
81033-102GUAIFENESIN LIQUID [KESIN PHARMA CORPORATION]1Current NDC, 1 package rows20250406_31b8ad0a-3637-03db-e063-6394a90acdc3.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 93 of 180 · 3,583 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
VANACOF DMDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDEGM Pharmaceuticals, INC2ed699f2-d004-4fa9-8042-6c85a9ff69b62025-11-03WarningsExact identifier
application number: M012
Geri DrylDIPHENHYDRAMINE HCLVERITYRX, LLC42a05f69-0599-5571-e063-6394a90a37d32025-11-02WarningsExact identifier
application number: M012
M-DrylDIPHENHYDRAMINE HYDROCHLORIDEVERITYRX, LLC42a0e577-a1b6-2c16-e063-6294a90af8e32025-11-02WarningsExact identifier
application number: M012
Severe Sinus Congestion and PainACETAMINOPHEN, GUAIFENESIN, PHENYLEPHRINEShield Pharmaceuticals Corpc296efd0-5030-4a26-a9b0-e66423d995dc2025-10-31WarningsExact identifier
application number: M012
Daytime Cold and Flu Max Maximum Strength SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLTopco Associates, LLCf7ebe482-cb22-4517-8463-3432cf60071d2025-10-31WarningsExact identifier
application number: M012
Nighttime Cold and Flu Max SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCLTopco Associates, LLC787bff76-0ee2-4e7e-b908-876e4a3e3bfc2025-10-31WarningsExact identifier
application number: M012
Honey Lemon Cough DropsMENTHOLTrader Joe's Company647dadae-f37a-8399-e053-2991aa0aedb32025-10-31WarningsExact identifier
application number: M012
Family Care SalineSODIUM CHLORIDEUnited Exchange Corp.06737393-d4ae-3e7b-e063-6394a90ac19f2025-10-31WarningsExact identifier
application number: M012
QUALITY CHOICE Maximum Strength Daytime Cold and FluACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, PHENYLEPHRINE HYDROCHLORIDEChain Drug Marketing Association, Inc.40416ff5-06e1-97dd-e063-6394a90a20462025-10-30WarningsExact identifier
application number: M012
Robitussin Maximum Strength Nighttime Cough DMDEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATEHaleon US Holdings LLC44feee2f-25bc-48d4-8e13-db1d9daaaa902025-10-30WarningsExact identifier
application number: M012
Robitussin Day and Night Cough Relief DM MaxDEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, DOXYLAMINE SUCCINATEHaleon US Holdings LLCb3d02c91-8f79-4eb4-a378-1072474c572c2025-10-30WarningsExact identifier
application number: M012
ROBITUSSIN MAXIMUM STRENGTH COUGH PLUS CHEST CONGESTION DMDEXTROMETHORPHAN HBR, GUAIFENESINHaleon US Holdings LLCf1d022dd-c2ca-497f-87d5-9ef3e20e8ea72025-10-30WarningsExact identifier
application number: M012
EndalTRIPROLIDINE HCL, DEXTROMETHORPHAN HBRPoly Pharmaceuticals, Inc.fc5401e2-ed65-72e7-e053-6294a90a81f32025-10-30WarningsExact identifier
application number: M012
daytimeACETAMINOPHEN, DEXTROMETHORPHAN HBR, PHENYLEPHRINE HCLPublix Super Markets Incc7cef266-46fc-49ab-a2e7-54fc562986592025-10-30WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HYDROCHLORIDESAM'S WEST INC16592ad7-b7cb-0837-e063-6394a90ae0592025-10-29WarningsExact identifier
application number: M012
Maximum Strength Severe Congestion and CoughDEXTROMETHORPHAN HBR, GUAIFENESIN, AND PHENYLEPHRINE HCLSAFEWAY013b94a1-26c7-4371-981a-d1b9d7fd1c982025-10-29WarningsExact identifier
application number: M012
Better LivingPHENYLEPHRINE HYDROCHLORIDEBETTER LIVING BRANDS LLCaea0db7f-e01a-4d8e-9c20-4a5ef4a905d12025-10-29WarningsExact identifier
application number: M012
AXIM DayTime - Night Time 72 SoftgelsACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HYDROCHLORIDEVIVUNT PHARMA LLCde9eb2d5-ba51-4637-e053-2995a90a04512025-10-29WarningsExact identifier
application number: M012
Dollar General Vapor SteamCAMPHOR (SYNTHETIC)DOLGENCORP, LLC86d0f3ac-1359-c2f9-e053-2a91aa0a35d02025-10-29WarningsExact identifier
application number: M012
Allergy ReliefDIPHENHYDRAMINE HCLStrategic Sourcing Services LLC5d628b09-c257-4369-8ddb-47554d83c0d82025-10-29WarningsExact identifier
application number: M012

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310604guaiFENesin 100 MG in 5 mL Oral SolutionPSN365c01b7-a197-4876-85fc-42204f787e3a7
310604guaifenesin 20 MG/ML Oral SolutionSCD365c01b7-a197-4876-85fc-42204f787e3a7
310604guaifenesin 100 MG per 5 ML Oral SolutionSY365c01b7-a197-4876-85fc-42204f787e3a7
310604guaifenesin 100 MG per 5 ML Oral SyrupSY365c01b7-a197-4876-85fc-42204f787e3a7
310604guaifenesin 200 MG per 10 ML Oral SolutionSY365c01b7-a197-4876-85fc-42204f787e3a7
310604guaifenesin 300 MG per 15 ML Oral SolutionSY365c01b7-a197-4876-85fc-42204f787e3a7
310604guaifenesin 400 MG per 20 ML Oral SolutionSY365c01b7-a197-4876-85fc-42204f787e3a7
310604guaiFENesin 100 MG in 5 mL Oral SolutionPSN31b8ad0a-3637-03db-e063-6394a90acdc31
310604guaifenesin 20 MG/ML Oral SolutionSCD31b8ad0a-3637-03db-e063-6394a90acdc31
310604guaifenesin 100 MG per 5 ML Oral SolutionSY31b8ad0a-3637-03db-e063-6394a90acdc31
310604guaifenesin 100 MG per 5 ML Oral SyrupSY31b8ad0a-3637-03db-e063-6394a90acdc31
310604guaifenesin 200 MG per 10 ML Oral SolutionSY31b8ad0a-3637-03db-e063-6394a90acdc31
310604guaifenesin 300 MG per 15 ML Oral SolutionSY31b8ad0a-3637-03db-e063-6394a90acdc31
310604guaifenesin 400 MG per 20 ML Oral SolutionSY31b8ad0a-3637-03db-e063-6394a90acdc31

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
81033-102-05810330102055 mL in 1 CUP, UNIT-DOSE5 mlHistorical
81033-102-108103301021010 mL in 1 CUP, UNIT-DOSE10 mlHistorical
81033-102-1681033010216473 mL in 1 BOTTLE (81033-102-16) 473 ml2025-04-01NoNoCurrent
81033-102-518103301025150 CUP, UNIT-DOSE in 1 CARTON (81033-102-51) / 5 mL in 1 CUP, UNIT-DOSE (81033-102-05) 2023-11-20NoNoCurrent
81033-102-528103301025250 CUP, UNIT-DOSE in 1 CARTON (81033-102-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-102-10) 2023-11-20NoNoCurrent