NDC 41167-0101-01 - Dulcolax Simulant Laxative
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 41167-0101
- Requested NDC
- 41167-0101-01
- Package NDCs from labels
- 41167-0101-0, 41167-0101-1, 41167-0101-2, 41167-0101-3, 41167-0101-4, 41167-0101-5, 41167-0101-6, 41167-0101-7, 41167-0101-01
- Manufacturer
- Chattem, Inc.
- Effective date
- 2025-04-01
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dulcolax Stimulant Laxative CMP-CHA | Chattem, Inc. | 2025-04-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 41167-0101-0 | Dulcolax Simulant Laxative | 8 in 1 BLISTER PACK | TABLET, FILM COATED | 8 | 8 | |
| 41167-0101-0 | Dulcolax Simulant Laxative | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 8 | |
| 41167-0101-1 | Dulcolax Simulant Laxative | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 8 | |
| 41167-0101-1 | Dulcolax Simulant Laxative | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 8 | |
| 41167-0101-2 | Dulcolax Simulant Laxative | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 8 | |
| 41167-0101-2 | Dulcolax Simulant Laxative | 25 in 1 BLISTER PACK | TABLET, FILM COATED | 25 | 8 | |
| 41167-0101-3 | Dulcolax Simulant Laxative | 25 in 1 BLISTER PACK | TABLET, FILM COATED | 25 | 8 | |
| 41167-0101-3 | Dulcolax Simulant Laxative | 2 in 1 CARTON | TABLET, FILM COATED | 2 | 8 | |
| 41167-0101-4 | Dulcolax Simulant Laxative | 25 in 1 BLISTER PACK | TABLET, FILM COATED | 25 | 8 | |
| 41167-0101-4 | Dulcolax Simulant Laxative | 4 in 1 CARTON | TABLET, FILM COATED | 4 | 8 | |
| 41167-0101-5 | Dulcolax Simulant Laxative | 8 in 1 CARTON | TABLET, FILM COATED | 8 | 8 | |
| 41167-0101-5 | Dulcolax Simulant Laxative | 25 in 1 BLISTER PACK | TABLET, FILM COATED | 25 | 8 | |
| 41167-0101-6 | Dulcolax Simulant Laxative | 3 in 1 CARTON | TABLET, FILM COATED | 3 | 8 | |
| 41167-0101-6 | Dulcolax Simulant Laxative | 10 in 1 BLISTER PACK | TABLET, FILM COATED | 10 | 8 | |
| 41167-0101-7 | Dulcolax Simulant Laxative | 1 in 1 CARTON | TABLET, FILM COATED | 1 | 8 | |
| 41167-0101-7 | Dulcolax Simulant Laxative | 6 in 1 BLISTER PACK | TABLET, FILM COATED | 6 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 41167-0101 | DULCOLAX SIMULANT LAXATIVE (BISACODYL) TABLET, FILM COATED [CHATTEM, INC.] | 8 | Current NDC, Legacy NDC, 16 package rows | 20250501_d285651b-7ccc-4ae5-a862-7a38dffefa28.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sterile Eyesaline Eyewash | STERILE EYESALINE EYEWASH | Protective Industrial Products, Inc. | 55a290e8-8310-8be4-e063-6394a90abdce | 2026-07-02 | Warnings | 059QF0KO0R |
| Eyesaline Emergency Eyewash | PURIFIED WATER | Protective Industrial Products, Inc. | 55a261c2-725d-6765-e063-6294a90a3260 | 2026-07-02 | Warnings | 059QF0KO0R |
| Remodulin | TREPROSTINIL | United Therapeutics Corporation | 6c80bb38-e8db-4138-9f0d-dbbf9c673185 | 2026-07-02 | Warnings, Adverse reactions | 059QF0KO0R |
| Calamine Plus Pramoxine HCl | CALAMINE PLUS SPRAY | Target Corporation | 36602b7a-99c0-f6a4-e063-6294a90a8758 | 2026-06-29 | Warnings | 1K09F3G675 |
| Walgreens Gentle Laxative | BISACODYL SUPPOSITORY | Walgreens | 20c43036-830b-0e1d-e063-6394a90adf5f | 2026-06-25 | Warnings | 10X0709Y6I |
| CalaSoothe | CALAMINE, MENTHOL, AND ZINC OXIDE | Dynarex Corporation | 54f12005-acfe-4821-e063-6394a90ac304 | 2026-06-24 | Warnings | 1K09F3G675 |
| Fendall 2000 Pure Flow | PURIFIED WATER | Honeywell Safety Products USA, Inc. | 37dead3e-60cb-88ae-e063-6294a90a8f70 | 2026-06-24 | Warnings | 059QF0KO0R |
| Womens Laxative | WOMENS LAXTIVE | Allegiant Health | 549a11d1-a096-4c22-96b4-2d4f54f46022 | 2026-06-24 | Warnings | 308753 10X0709Y6I |
| Bacteriostatic Water | BACTERIOSTATIC WATER | Fujian Genohope Biotech Ltd. | 54f66b82-c9e5-a2bc-e063-6394a90adbbc | 2026-06-23 | 059QF0KO0R | |
| Gentle Laxative | BISACODYL | Chain Drug Marketing Association, Inc. | 8bbc8ad6-4508-431a-a547-c11c3129243d | 2026-06-22 | Warnings | 308753 10X0709Y6I |
| Rohto Cool Relief | NAPHAZOLINE HYDROCHLORIDE, POLYSORBATE 80 | The Mentholatum Company | dc8f1ff3-87ae-47ca-815f-5a0e34f8cf30 | 2026-06-19 | Warnings | 6OZP39ZG8H |
| Rohto Sun and Sport | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 8bcc8882-b886-4b55-9bc4-d4b92a41358f | 2026-06-19 | Warnings | 3NXW29V3WO |
| Rohto Dual Light Relief | HYPROMELLOSE, POVIDONE | The Mentholatum Company | 1b597f83-d7f1-cf93-e063-6394a90a99f7 | 2026-06-19 | Warnings | 3NXW29V3WO |
| laxative | BISACODYL | Publix Super Markets Inc | 04279d2b-2bb7-4d74-86a4-476b5c08aa05 | 2026-06-18 | Warnings | 308753 10X0709Y6I |
| Humalog | INSULIN LISPRO | Eli Lilly and Company | c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f | 2026-06-16 | Warnings, Adverse reactions | 059QF0KO0R |
| Gentle Laxative | BISACODYL | Family Dollar Services Inc | cffa0a9d-8353-432c-b098-318a2c43d711 | 2026-06-16 | Warnings | 308753 10X0709Y6I |
| Laxative | BISACODYL | Family Dollar Services Inc | af976b4a-f444-49f4-9843-99638ed07d36 | 2026-06-16 | Warnings | 308753 10X0709Y6I |
| Calamine, Pramoxind HCl | CALAMINE, PRAMOXIND HCL | H E B | 4a7a0b09-d9bc-e752-e063-6394a90a9f2c | 2026-06-15 | Warnings, Adverse reactions | 1K09F3G675 |
| Calamine, Zinc Oxide | CALAMINE, ZINC OXIDE | H E B | 4a79259e-64ac-d187-e063-6294a90a78db | 2026-06-15 | Warnings, Adverse reactions | 1K09F3G675 |
| Gentle Laxative | BISACODYL | United Natural Foods, Inc. dba UNFI | 1daeccb6-b8ab-43dc-a8fd-07ffc1fc1138 | 2026-06-15 | Warnings | 308753 10X0709Y6I |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.