| Product NDC: | 37808-469 | 
| Proprietary Name: | rx act stomach relief | 
| Non Proprietary Name: | Bismuth subsalicylate | 
| Active Ingredient(s): | 262 mg/1 & nbsp; Bismuth subsalicylate | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET, CHEWABLE | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 37808-469 | 
| Labeler Name: | H E B | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part335 | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 19941108 | 
| Package NDC: | 37808-469-65 | 
| Package Description: | 5 BLISTER PACK in 1 CARTON (37808-469-65) > 6 TABLET, CHEWABLE in 1 BLISTER PACK | 
| NDC Code | 37808-469-65 | 
| Proprietary Name | rx act stomach relief | 
| Package Description | 5 BLISTER PACK in 1 CARTON (37808-469-65) > 6 TABLET, CHEWABLE in 1 BLISTER PACK | 
| Product NDC | 37808-469 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Bismuth subsalicylate | 
| Dosage Form Name | TABLET, CHEWABLE | 
| Route Name | ORAL | 
| Start Marketing Date | 19941108 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | H E B | 
| Substance Name | BISMUTH SUBSALICYLATE | 
| Strength Number | 262 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes |