| Product NDC: | 59640-016 | 
| Proprietary Name: | Peptic Relief | 
| Non Proprietary Name: | Bismuth Subsalicylate | 
| Active Ingredient(s): | 262 mg/15mL & nbsp; Bismuth Subsalicylate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | SUSPENSION | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 59640-016 | 
| Labeler Name: | H.E.B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part335 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20090209 | 
| Package NDC: | 59640-016-08 | 
| Package Description: | 237 mL in 1 BOTTLE, PLASTIC (59640-016-08) | 
| NDC Code | 59640-016-08 | 
| Proprietary Name | Peptic Relief | 
| Package Description | 237 mL in 1 BOTTLE, PLASTIC (59640-016-08) | 
| Product NDC | 59640-016 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Bismuth Subsalicylate | 
| Dosage Form Name | SUSPENSION | 
| Route Name | ORAL | 
| Start Marketing Date | 20090209 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H.E.B | 
| Substance Name | BISMUTH SUBSALICYLATE | 
| Strength Number | 262 | 
| Strength Unit | mg/15mL | 
| Pharmaceutical Classes |