ROBITUSSIN COUGH PLUS CHEST CONGESTION DM

Product NDC
0031-8757
11-digit product format
000318757
Labeler code
0031
Product ID
0031-8757_159a64fb-02c1-1365-e063-6394a90af696
Type
HUMAN OTC DRUG
Nonproprietary name
dextromethorphan hydrobromide and guaifenesin
Dosage form
SOLUTION
Route
ORAL
Labeler
Haleon US Holdings LLC
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-06-01
Substance
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Active strength
20; 200 mg/20mL; mg/20mL
Pharmacologic classes
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]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
ROBITUSSIN COUGH PLUS CHEST CONGESTION DM
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
DEXTROMETHORPHAN HYDROBROMIDE20 mg/20mL
GUAIFENESIN200 mg/20mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii9D2RTI9KYH, 495W7451VQ
Rxcui1790650

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bf324df6-7127-7deb-def5-2681c136cd03Product name320250325
43a1ed49-eae2-4840-8075-cb4b33478540Product name120230425
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
ba088a92-ab5e-b2d4-e908-f5ea691b7587Product name720210201
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
4fe95224-f543-4dbb-9445-8cca122b48c8Product name120150609
e8718272-64cb-4436-969b-176c3067c8f4Product name120150609
106ff02a-57e1-4c4c-a307-fd582ff4e311Product name120150212
76633df9-0d59-4b88-03ed-21dee1b966f8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0031-8757-12ROBITUSSIN COUGH PLUS CHEST CONGESTION DM1 in 1 CARTONSOLUTION18
0031-8757-12ROBITUSSIN COUGH PLUS CHEST CONGESTION DM118 mL in 1 BOTTLESOLUTION1188
0031-8757-18ROBITUSSIN COUGH PLUS CHEST CONGESTION DM237 mL in 1 BOTTLESOLUTION2378
0031-8757-18ROBITUSSIN COUGH PLUS CHEST CONGESTION DM1 in 1 CARTONSOLUTION18

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0031-8757-12ML - Milliliter0031-87578c224c3e-6c97-47ef-8655-fe8aabff8bc112019-02-13
0031-8757-18ML - Milliliter0031-8757ac2e0a8a-80d8-4a84-a92f-da412510a1dd12019-01-24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0031-8757ROBITUSSIN COUGH PLUS CHEST CONGESTION DM (DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN) SOLUTION [HALEON US HOLDINGS LLC]8Current NDC, Legacy NDC, 4 package rows20240410_4908b326-e1da-44ca-8087-7e41a16c27b0.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1790650dextromethorphan HBr 10 MG / guaiFENesin 100 MG in 10 mL Oral SolutionPSN4908b326-e1da-44ca-8087-7e41a16c27b08
1790650dextromethorphan hydrobromide 1 MG/ML / guaifenesin 10 MG/ML Oral SolutionSCD4908b326-e1da-44ca-8087-7e41a16c27b08
1790650dextromethorphan HBr 10 MG / guaifenesin 100 MG per 10 ML Oral SolutionSY4908b326-e1da-44ca-8087-7e41a16c27b08
1790650dextromethorphan HBr 20 MG / guaifenesin 200 MG per 20 ML Oral SolutionSY4908b326-e1da-44ca-8087-7e41a16c27b08
1790650dextromethorphan HBr 5 MG / guaifenesin 50 MG per 5 ML Oral SolutionSY4908b326-e1da-44ca-8087-7e41a16c27b08

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0031-8757-12000318757121 BOTTLE in 1 CARTON (0031-8757-12) / 118 mL in 1 BOTTLE1 bottle2018-06-010000-00-00NoNoCurrent
0031-8757-18000318757181 BOTTLE in 1 CARTON (0031-8757-18) / 237 mL in 1 BOTTLE1 bottle2018-06-010000-00-00NoNoCurrent