FDA.reportPublic FDA data

Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu Nighttime

Product NDC
0031-0101
11-digit product format
000310101
Labeler code
0031
Product ID
0031-0101_0f9df094-b106-76fc-e063-6294a90a6a18
Type
HUMAN OTC DRUG
Nonproprietary name
acetaminophen, diphenhydramine hcl
Dosage form
LIQUID
Route
ORAL
Labeler
Haleon US Holdings LLC
Application
M012
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-15
Substance
ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active strength
650; 25 mg/20mL; mg/20mL
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu Nighttime
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN650 mg/20mL
DIPHENHYDRAMINE HYDROCHLORIDE25 mg/20mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D, TC2D6JAD40
Rxcui2374554

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0031-0101-04Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu Nighttime1 in 1 CARTONLIQUID11
0031-0101-04Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu Nighttime118 mL in 1 BOTTLELIQUID1181

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0031-0101ROBITUSSIN MAXIMUM STRENGTH SEVERE MULTI-SYMPTOM COUGH COLD FLU NIGHTTIME (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) LIQUID [HALEON US HOLDINGS LLC]1Current NDC, 2 package rows20240215_721bfee2-0d3d-4d8b-beee-1ea83064d1c8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2374554acetaminophen 650 MG / diphenhydrAMINE HCl 25 MG in 20 mL Oral SolutionPSN721bfee2-0d3d-4d8b-beee-1ea83064d1c81
2374554acetaminophen 32.5 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML Oral SolutionSCD721bfee2-0d3d-4d8b-beee-1ea83064d1c81
2374554acetaminophen 650 MG / diphenhydramine HCl 25 MG per 20 mL Oral SolutionSY721bfee2-0d3d-4d8b-beee-1ea83064d1c81
2374554APAP 32.5 MG/ML / diphenhydramine hydrochloride 1.25 MG/ML Oral SolutionSY721bfee2-0d3d-4d8b-beee-1ea83064d1c81

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
0031-0101-04000310101041 BOTTLE in 1 CARTON (0031-0101-04) / 118 mL in 1 BOTTLE1 bottle2024-02-15NoNoCurrent