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NDC 11673-0182-52 BISACODYL 5 mg/1 Details
BISACODYL 5 mg/1
BISACODYL is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by TARGET CORPORATION. The primary component is BISACODYL.
MedlinePlus Drug Summary
Bisacodyl is used on a short-term basis to treat constipation. It also is used to empty the bowels before surgery and certain medical procedures. Bisacodyl is in a class of medications called stimulant laxatives. It works by increasing activity of the intestines to cause a bowel movement.
Related Packages: 11673-0182-52Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Bisacodyl
Product Information
| NDC | 11673-0182 |
|---|---|
| Product ID | 11673-182_9cbeae92-020a-3931-e053-2995a90ac96b |
| Associated GPIs | 43998903350920 |
| GCN Sequence Number | 053178 |
| GCN Sequence Number Description | DM/acetaminophen/doxylamine LIQUID 30-12.5/30 ORAL |
| HIC3 | B4G |
| HIC3 Description | NON-OPIOID ANTITUS-1ST GEN ANTIHIST-ANALGESIC COMB |
| GCN | 20556 |
| HICL Sequence Number | 025663 |
| HICL Sequence Number Description | DEXTROMETHORPHAN HBR/ACETAMINOPHEN/DOXYLAMINE |
| Brand/Generic | Generic |
| Proprietary Name | BISACODYL |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | BISCODYL |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, COATED |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | BISACODYL |
| Labeler Name | TARGET CORPORATION |
| Pharmaceutical Class | Increased Large Intestinal Motility [PE], Stimulant Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part334 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 11673-0182-52 (11673018252)
| NDC Package Code | 11673-182-52 |
|---|---|
| Billing NDC | 11673018252 |
| Package | 25 TABLET, COATED in 1 BLISTER PACK (11673-182-52) |
| Marketing Start Date | 2020-02-04 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL 8ed281d5-b17e-e3bb-e053-2995a90a2590 Details
SPL UNCLASSIFIED SECTION
Acacia, Anhydrous CalciumSulfate, Anhydrous Lactose, Carnauba Wax, Colloidal Silicon Dioxide, Corn Starch,
D&C Yellow #10 Aluminum Lake, Gelatin, Iron Oxide, Iron Oxide Black, Iron Oxide Yellow(Iron Oxide Ochre),
FD&C Yellow #6, Magnesium Stearate, Microcrystalline Cellulose, Polyethylene Glycol (PEG) 400,
Polyvinyl Acetate Phthalates, Povidone, Shellac, Sodium Starch Glycolate, Stearic Acid, Sugar, Talc, Titanium Dioxide
SPL UNCLASSIFIED SECTION
SPL UNCLASSIFIED SECTION
SPL UNCLASSIFIED SECTION
WARNINGS
Warning: Do not use if you cannot swallow without chewing.
Ask a doctor before use if you have: stomach pain, nausea or vomiting; A sudden change in bowel habits that lasts more than two weeks.
When using this product: Do not chew or crush tablet(s); Do not use within 1 hour after taking an antacid or milk; Do not use this product if you have stomach discomfort, faintness or cramps.
SPL UNCLASSIFIED SECTION
INGREDIENTS AND APPEARANCE
| BISACODYL
biscodyl tablet, coated |
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| Labeler - TARGET CORPORATION (006961700) |
| Registrant - TIME CAP LABORATORIES, INC (037052099) |
| Establishment | |||
| Name | Address | ID/FEI | Business Operations |
|---|---|---|---|
| TIME CAP LABORATORIES, INC. | 037052099 | manufacture(11673-182) | |