dg health childrens mucus relief

Product NDC
55910-839
11-digit product format
559100839
Labeler code
55910
Product ID
55910-839_a133bb1f-1125-4bd1-8597-a6d18896990e
Type
HUMAN OTC DRUG
Nonproprietary name
dextromethorphan HBr, guaifenesin, phenylephrine HCl
Dosage form
SOLUTION
Route
ORAL
Labeler
Dolgencorp Inc
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-05-06
Marketing end
0000-00-00
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength
5 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classes
Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct55910-839DDiscontinued by firm2026-10-20
excluded packagepackage55910-83955910-839-26DDiscontinued by firm2026-10-20

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproduct55910-839DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage55910-83955910-839-26DDiscontinued by firmexcluded / ndc_excluded.zipd630ba8d3edf…732f749b63fb…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e4e263da-1c53-440f-bb80-b7a575843b5aProduct name120260313
d2168cac-a261-415a-9c78-3522859fa720Product name320251124
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
05a8cdd1-eeb8-409e-b938-0778225eca7dProduct name420250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9Product name820250220
f489e8f3-5c9e-4818-b539-a73587edcfc7Product name220240229
0f7ae452-206d-4fc4-868d-56fc47074084Product name120231011
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
b5abe2e3-39a1-43eb-9bff-f3c1653fe3dfProduct name220190930
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814Product name320150910
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212
42f3c020-f1b3-89bc-7bdc-e1f10e680485Product name120140508
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
e949165d-714d-e548-2b76-0cb5def16f30Product name120140508

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
DEXTROMETHORPHAN HYDROBROMIDEACTIVE INGREDIENT9D2RTI9KYHDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
GUAIFENESINACTIVE INGREDIENT495W7451VQDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
PHENYLEPHRINE HYDROCHLORIDEACTIVE INGREDIENT04JA59TNSJDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
DEXTROMETHORPHANACTIVE MOIETY7355X3ROTSDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
GUAIFENESINACTIVE MOIETY495W7451VQDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
PHENYLEPHRINEACTIVE MOIETY1WS297W6MVDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
ANHYDROUS CITRIC ACIDINACTIVE INGREDIENTXF417D3PSLDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
EDETATE DISODIUMINACTIVE INGREDIENT7FLD91C86KDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
FD&C RED NO. 40INACTIVE INGREDIENTWZB9127XOADG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
GLYCERININACTIVE INGREDIENTPDC6A3C0OXDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3DG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
SODIUM BENZOATEINACTIVE INGREDIENTOJ245FE5EUDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
SODIUM CITRATEINACTIVE INGREDIENT1Q73Q2JULRDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
SORBITOLINACTIVE INGREDIENT506T60A25RDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
SUCRALOSEINACTIVE INGREDIENT96K6UQ3ZD4DG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
WATERINACTIVE INGREDIENT059QF0KO0RDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2
XANTHAN GUMINACTIVE INGREDIENTTTV12P4NEEDG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-839DG HEALTH CHILDRENS MUCUS RELIEF (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCL) SOLUTION [DOLGENCORP INC]5Legacy NDC20241114_2832857c-c2a2-4074-b382-10c54317b4df.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
55910-839-26559100839261 BOTTLE in 1 CARTON (55910-839-26) > 118 mL in 1 BOTTLE1 bottle2015-05-060000-00-00NoNoCurrent