FDA.reportPublic FDA data

OneLAX SENNA

Product NDC
17856-8127
11-digit product format
178568127
Labeler code
17856
Product ID
17856-8127_40202c81-a84f-63e9-e063-6294a90a8947
Type
HUMAN OTC DRUG
Nonproprietary name
SENNA
Dosage form
SYRUP
Route
ORAL
Labeler
Atlantic Biologicals Corp.
Application
M007
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-02-06
Substance
SENNOSIDES A AND B
Active strength
417.12 mg/237mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SENNOSIDES A AND B417.12 mg/237mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1B5FPI42EN
Rxcui702311

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-8127-2OneLAX SENNA50 in 1 CASESYRUP501
17856-8127-2OneLAX SENNA5 mL in 1 CUP, UNIT-DOSESYRUP51

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
702311sennosides 8.8 MG in 5 mL Oral SolutionPSN40202c76-4273-88fd-e063-6394a90a07b21
702311sennosides, USP 1.76 MG/ML Oral SolutionSCD40202c76-4273-88fd-e063-6394a90a07b21
702311sennosides 8.8 MG per 5 mL Oral SyrupSY40202c76-4273-88fd-e063-6394a90a07b21
702311sennosides, USP 26.4 MG per 15 ML Oral SolutionSY40202c76-4273-88fd-e063-6394a90a07b21
702311sennosides, USP 8.8 MG per 5 ML Oral SolutionSY40202c76-4273-88fd-e063-6394a90a07b21

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
17856-8127-21785681270250 CUP, UNIT-DOSE in 1 CASE (17856-8127-2) / 5 mL in 1 CUP, UNIT-DOSE2025-10-10NoNoHistorical