onelax senna

Generic: senna

Labeler: atlantic biologicals corp.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name onelax senna
Generic Name senna
Labeler atlantic biologicals corp.
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

sennosides a and b 417.12 mg/237mL

Manufacturer
Atlantic Biologicals Corp.

Identifiers & Regulatory

Product NDC 17856-8127
Product ID 17856-8127_40202c81-a84f-63e9-e063-6294a90a8947
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2024-02-06

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 178568127
Hyphenated Format 17856-8127

Supplemental Identifiers

RxCUI
702311
UNII
1B5FPI42EN

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name onelax senna (source: ndc)
Generic Name senna (source: ndc)
Application Number M007 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 417.12 mg/237mL
source: ndc
Packaging
  • 50 CUP, UNIT-DOSE in 1 CASE (17856-8127-2) / 5 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (1)

Ingredients (1)

sennosides a and b (417.12 mg/237mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40202c81-a84f-63e9-e063-6294a90a8947", "openfda": {"unii": ["1B5FPI42EN"], "rxcui": ["702311"], "spl_set_id": ["40202c76-4273-88fd-e063-6394a90a07b2"], "manufacturer_name": ["Atlantic Biologicals Corp."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (17856-8127-2)  / 5 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-8127-2", "marketing_start_date": "20251010"}], "brand_name": "OneLAX SENNA", "product_id": "17856-8127_40202c81-a84f-63e9-e063-6294a90a8947", "dosage_form": "SYRUP", "product_ndc": "17856-8127", "generic_name": "SENNA", "labeler_name": "Atlantic Biologicals Corp.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OneLAX SENNA", "active_ingredients": [{"name": "SENNOSIDES A AND B", "strength": "417.12 mg/237mL"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240206", "listing_expiration_date": "20261231"}