dulcolax laxative

Generic: bisacodyl

Labeler: chattem, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name dulcolax laxative
Generic Name bisacodyl
Labeler chattem, inc.
Dosage Form SUPPOSITORY
Routes
RECTAL
Active Ingredients

bisacodyl 10 mg/1

Manufacturer
Chattem, Inc.

Identifiers & Regulatory

Product NDC 41167-0210
Product ID 41167-0210_d39ca8c0-d92a-4c16-a35e-efa8acc21aa5
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2026-12-31
Marketing Start 2019-06-04

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 411670210
Hyphenated Format 41167-0210

Supplemental Identifiers

RxCUI
198509 209601
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 dulcolax laxative (source: ndc)
Generic Name bisacodyl (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
RECTAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (41167-0210-1) / 4 SUPPOSITORY in 1 BLISTER PACK
  • 2 BLISTER PACK in 1 CARTON (41167-0210-2) / 4 SUPPOSITORY in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (41167-0210-3) / 4 SUPPOSITORY in 1 BLISTER PACK
  • 7 BLISTER PACK in 1 CARTON (41167-0210-5) / 4 SUPPOSITORY in 1 BLISTER PACK
source: ndc

Packages (4)

41167-0210-1 1 BLISTER PACK in 1 CARTON (41167-0210-1) / 4 SUPPOSITORY in 1 BLISTER PACK 41167-0210-2 2 BLISTER PACK in 1 CARTON (41167-0210-2) / 4 SUPPOSITORY in 1 BLISTER PACK 41167-0210-3 4 BLISTER PACK in 1 CARTON (41167-0210-3) / 4 SUPPOSITORY in 1 BLISTER PACK 41167-0210-5 7 BLISTER PACK in 1 CARTON (41167-0210-5) / 4 SUPPOSITORY in 1 BLISTER PACK

Ingredients (1)

bisacodyl (10 mg/1)

Linked Drug Pages (1)

Dulcolax Laxative ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["RECTAL"], "spl_id": "d39ca8c0-d92a-4c16-a35e-efa8acc21aa5", "openfda": {"nui": ["N0000009371", "N0000175812", "N0000009871"], "unii": ["10X0709Y6I"], "rxcui": ["198509", "209601"], "spl_set_id": ["016a4920-77a7-4ac3-8d9d-fd2f564dfee6"], "pharm_class_pe": ["Increased Large Intestinal Motility [PE]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "pharm_class_epc": ["Stimulant Laxative [EPC]"], "manufacturer_name": ["Chattem, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (41167-0210-1)  / 4 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "41167-0210-1", "marketing_start_date": "20190604"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (41167-0210-2)  / 4 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "41167-0210-2", "marketing_start_date": "20190604"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (41167-0210-3)  / 4 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "41167-0210-3", "marketing_start_date": "20190604"}, {"sample": false, "description": "7 BLISTER PACK in 1 CARTON (41167-0210-5)  / 4 SUPPOSITORY in 1 BLISTER PACK", "package_ndc": "41167-0210-5", "marketing_start_date": "20190604"}], "brand_name": "Dulcolax Laxative", "product_id": "41167-0210_d39ca8c0-d92a-4c16-a35e-efa8acc21aa5", "dosage_form": "SUPPOSITORY", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Stimulant Laxative [EPC]", "Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]"], "product_ndc": "41167-0210", "generic_name": "Bisacodyl", "labeler_name": "Chattem, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dulcolax Laxative", "active_ingredients": [{"name": "BISACODYL", "strength": "10 mg/1"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190604", "listing_expiration_date": "20261231"}