FDA.reportPublic FDA data

GUAIFENESIN

Product NDC
0121-1744
11-digit product format
001211744
Labeler code
0121
Product ID
0121-1744_25a970c7-0016-4f22-9e94-1e20e1319e3e
Type
HUMAN OTC DRUG
Nonproprietary name
GUAIFENESIN
Dosage form
SOLUTION
Route
ORAL
Labeler
PAI Holdings, LLC dba PAI Pharma
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2002-09-01
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

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 Identifiers#

Field, Values table
FieldValues
Unii495W7451VQ
Rxcui310604

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0121-1744-00GUAIFENESIN10 in 1 CASESOLUTION109
0121-1744-00GUAIFENESIN10 in 1 TRAYSOLUTION109
0121-1744-05GUAIFENESIN5 mL in 1 CUP, UNIT-DOSESOLUTION59

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0121-1744-00ML - Milliliter0121-1744171bdc6a-7b5f-45a7-87e1-b202b3ef5ad412018-01-12
0121-1744-05ML - Milliliter0121-174480ee20cf-4e2b-4882-bcd2-cbd2ec3f467112014-10-03
0121-1744-10ML - Milliliter0121-174429730dba-fb62-49e5-b8f8-98345a3002ea12014-10-03
0121-1744-15ML - Milliliter0121-17448868bbf3-ee16-4fa4-8362-f51827a901a012014-10-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GUAIFENESINACTIVE INGREDIENT495W7451VQGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
GUAIFENESINACTIVE MOIETY495W7451VQGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
ACESULFAME POTASSIUMINACTIVE INGREDIENT23OV73Q5G9GUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
FD&C GREEN NO. 3INACTIVE INGREDIENT3P3ONR6O1SGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOAGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
HYDROXYETHYL CELLULOSE (140 MPA.S AT 5%)INACTIVE INGREDIENT8136Y38GY5GUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULRGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2
WATERINACTIVE INGREDIENT059QF0KO0RGUAIFENESIN SOLUTION [PHARMACEUTICAL ASSOCIATES, INC.]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0121-1744GUAIFENESIN SOLUTION [PAI HOLDINGS, LLC DBA PAI PHARMA]9Current NDC, Legacy NDC, 3 package rows20241113_c2e53fb5-2798-47c8-9285-d1077d46e629.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310604guaiFENesin 100 MG in 5 mL Oral SolutionPSN888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaifenesin 20 MG/ML Oral SolutionSCD888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaifenesin 100 MG per 5 ML Oral SolutionSY888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaifenesin 100 MG per 5 ML Oral SyrupSY888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaifenesin 200 MG per 10 ML Oral SolutionSY888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaifenesin 300 MG per 15 ML Oral SolutionSY888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaifenesin 400 MG per 20 ML Oral SolutionSY888b6a2e-6631-4585-a7fe-eb122eb51b2310
310604guaiFENesin 100 MG in 5 mL Oral SolutionPSNc2e53fb5-2798-47c8-9285-d1077d46e6299
310604guaifenesin 20 MG/ML Oral SolutionSCDc2e53fb5-2798-47c8-9285-d1077d46e6299
310604guaifenesin 100 MG per 5 ML Oral SolutionSYc2e53fb5-2798-47c8-9285-d1077d46e6299
310604guaifenesin 100 MG per 5 ML Oral SyrupSYc2e53fb5-2798-47c8-9285-d1077d46e6299
310604guaifenesin 200 MG per 10 ML Oral SolutionSYc2e53fb5-2798-47c8-9285-d1077d46e6299
310604guaifenesin 300 MG per 15 ML Oral SolutionSYc2e53fb5-2798-47c8-9285-d1077d46e6299
310604guaifenesin 400 MG per 20 ML Oral SolutionSYc2e53fb5-2798-47c8-9285-d1077d46e6299

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0121-1744-000012117440010 TRAY in 1 CASE (0121-1744-00) / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-1744-05) 10 tray2002-09-010000-00-00NoNoCurrent
0121-1744-05001211744055 mL in 1 CUP, UNIT-DOSE5 mlHistorical
0121-1744-100012117441010 TRAY in 1 CASE (0121-1744-10) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE10 tray2002-09-010000-00-00NoNoCurrent
0121-1744-150012117441510 TRAY in 1 CASE (0121-1744-15) > 10 CUP, UNIT-DOSE in 1 TRAY > 15 mL in 1 CUP, UNIT-DOSE10 tray2002-09-010000-00-00NoNoCurrent