onelax

Generic: bisacodyl

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

Drug Facts

Product Profile

Brand Name onelax
Generic Name bisacodyl
Labeler akron pharma inc
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

bisacodyl 10 mg/1

Manufacturer
AKRON PHARMA INC

Identifiers & Regulatory

Product NDC 71399-8460
Product ID 71399-8460_42b7c75d-d66d-77f9-e063-6294a90a4e40
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M007
Listing Expiration 2026-12-31
Marketing Start 2024-09-13

Pharmacologic Class

Established (EPC)
stimulant laxative [epc]
Physiologic Effect
increased large intestinal motility [pe] stimulation large intestine fluid/electrolyte secretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713998460
Hyphenated Format 71399-8460

Supplemental Identifiers

RxCUI
198509
UPC
0371399846020
UNII
10X0709Y6I
NUI
N0000009371 N0000175812 N0000009871

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 (source: ndc)
Generic Name bisacodyl (source: ndc)
Application Number M007 (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 12 BLISTER PACK in 1 BOX (71399-8460-2) / 1 SUPPOSITORY in 1 BLISTER PACK
  • 50 BLISTER PACK in 1 BOX (71399-8460-5) / 1 SUPPOSITORY in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (1)

bisacodyl (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "42b7c75d-d66d-77f9-e063-6294a90a4e40", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "upc": ["0371399846020"], "unii": ["10X0709Y6I"], "rxcui": ["198509"], "spl_set_id": ["be4eeb4d-df29-45dc-94ff-933e52c8b6f6"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["AKRON PHARMA INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 BLISTER PACK in 1 BOX (71399-8460-2)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "71399-8460-2", "marketing_start_date": "20240913"}, {"sample": false, "description": "50 BLISTER PACK in 1 BOX (71399-8460-5)  / 1 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "71399-8460-5", "marketing_start_date": "20240913"}], "brand_name": "OneLAX", "product_id": "71399-8460_42b7c75d-d66d-77f9-e063-6294a90a4e40", "dosage_form": "SUPPOSITORY", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "71399-8460", "generic_name": "BISACODYL", "labeler_name": "AKRON PHARMA INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "OneLAX", "active_ingredients": [{"name": "BISACODYL", "strength": "10 mg/1"}], "application_number": "M007", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240913", "listing_expiration_date": "20261231"}