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NDC 36800-0710-24 Bismuth Subsalicylate 262 mg/1 Details
Bismuth Subsalicylate 262 mg/1
Bismuth Subsalicylate is a ORAL CAPSULE, GELATIN COATED in the HUMAN OTC DRUG category. It is labeled and distributed by TOPCO ASSOCIATES LLC. The primary component is BISMUTH SUBSALICYLATE.
MedlinePlus Drug Summary
Bismuth subsalicylate is used to treat diarrhea, heartburn, and upset stomach in adults and children 12 years of age and older. Bismuth subsalicylate is in a class of medications called antidiarrheal agents. It works by decreasing the flow of fluids and electrolytes into the bowel, reduces inflammation within the intestine, and may kill the organisms that can cause diarrhea.
Related Packages: 36800-0710-24Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Bismuth Subsalicylate
Product Information
| NDC | 36800-0710 |
|---|---|
| Product ID | 36800-710_0c071da6-bf8b-9261-e063-6294a90ab0c5 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Bismuth Subsalicylate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Bismuth Subsalicylate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | CAPSULE, GELATIN COATED |
| Route | ORAL |
| Active Ingredient Strength | 262 |
| Active Ingredient Units | mg/1 |
| Substance Name | BISMUTH SUBSALICYLATE |
| Labeler Name | TOPCO ASSOCIATES LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH DRUG |
| Application Number | M008 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 36800-0710-24 (36800071024)
| NDC Package Code | 36800-710-24 |
|---|---|
| Billing NDC | 36800071024 |
| Package | 2 BLISTER PACK in 1 CARTON (36800-710-24) / 12 CAPSULE, GELATIN COATED in 1 BLISTER PACK |
| Marketing Start Date | 2021-02-19 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |