onelax senna

Generic: senna

Labeler: akron pharma inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name onelax senna
Generic Name senna
Labeler akron pharma inc.
Dosage Form SYRUP
Routes
ORAL
Active Ingredients

sennosides a and b 417.12 mg/237mL

Manufacturer
Akron Pharma Inc.

Identifiers & Regulatory

Product NDC 71399-0027
Product ID 71399-0027_4227fa19-b935-0fbc-e063-6294a90ac342
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 713990027
Hyphenated Format 71399-0027

Supplemental Identifiers

RxCUI
702311
UPC
0371399002785
UNII
1B5FPI42EN

Packaging Origin

Original Packager
true

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
  • 237 mL in 1 BOTTLE (71399-0027-8)
source: ndc

Packages (1)

71399-0027-8 237 mL in 1 BOTTLE (71399-0027-8)

Ingredients (1)

sennosides a and b (417.12 mg/237mL)

Linked Drug Pages (1)

OneLAX SENNA ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4227fa19-b935-0fbc-e063-6294a90ac342", "openfda": {"upc": ["0371399002785"], "unii": ["1B5FPI42EN"], "rxcui": ["702311"], "spl_set_id": ["27fa8f54-ed84-4afd-8da3-8754da48643b"], "manufacturer_name": ["Akron Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (71399-0027-8)", "package_ndc": "71399-0027-8", "marketing_start_date": "20240206"}], "brand_name": "OneLAX SENNA", "product_id": "71399-0027_4227fa19-b935-0fbc-e063-6294a90ac342", "dosage_form": "SYRUP", "product_ndc": "71399-0027", "generic_name": "SENNA", "labeler_name": "Akron Pharma Inc.", "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"}