womens gentle laxative
Generic: bisacodyl
Labeler: chain drug marketing association incDrug Facts
Product Profile
Brand Name
womens gentle laxative
Generic Name
bisacodyl
Labeler
chain drug marketing association inc
Dosage Form
TABLET, DELAYED RELEASE
Routes
Active Ingredients
bisacodyl 5 mg/1
Manufacturer
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)
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63868573
Hyphenated Format
63868-573
Supplemental Identifiers
RxCUI
UPC
UNII
NUI
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 2 BLISTER PACK in 1 CARTON (63868-573-30) / 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Packages (1)
Ingredients (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"}