womens gentle laxative

Generic: bisacodyl

Labeler: chain drug marketing association inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name womens gentle laxative
Generic Name bisacodyl
Labeler chain drug marketing association inc
Dosage Form TABLET, DELAYED RELEASE
Routes
ORAL
Active Ingredients

bisacodyl 5 mg/1

Manufacturer
CHAIN DRUG MARKETING ASSOCIATION INC

Identifiers & Regulatory

Product NDC 63868-573
Product ID 63868-573_a520623c-946d-45da-a03c-76a10a3ed520
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Marketing Start 2020-02-17
Marketing End 2027-01-31

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 63868573
Hyphenated Format 63868-573

Supplemental Identifiers

RxCUI
308753
UPC
0635515988422
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 womens gentle laxative (source: ndc)
Generic Name bisacodyl (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (63868-573-30) / 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

bisacodyl (5 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a520623c-946d-45da-a03c-76a10a3ed520", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "upc": ["0635515988422"], "unii": ["10X0709Y6I"], "rxcui": ["308753"], "spl_set_id": ["5a6aa2df-bf69-465d-ba62-e660b13f16cd"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["CHAIN DRUG MARKETING ASSOCIATION INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (63868-573-30)  / 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "63868-573-30", "marketing_end_date": "20270131", "marketing_start_date": "20200217"}], "brand_name": "Womens Gentle Laxative", "product_id": "63868-573_a520623c-946d-45da-a03c-76a10a3ed520", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "63868-573", "generic_name": "Bisacodyl", "labeler_name": "CHAIN DRUG MARKETING ASSOCIATION INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Womens Gentle Laxative", "active_ingredients": [{"name": "BISACODYL", "strength": "5 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270131", "marketing_start_date": "20200217"}