Product NDC: | 0280-4095 |
Proprietary Name: | Alka-Seltzer Fruit Chews |
Non Proprietary Name: | calcium carbonate |
Active Ingredient(s): | 750 mg/1 & nbsp; calcium carbonate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0280-4095 |
Labeler Name: | Bayer HealthCare LLC, Consumer Care |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part331 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130315 |
Package NDC: | 0280-4095-60 |
Package Description: | 60 TABLET, CHEWABLE in 1 BOTTLE (0280-4095-60) |
NDC Code | 0280-4095-60 |
Proprietary Name | Alka-Seltzer Fruit Chews |
Package Description | 60 TABLET, CHEWABLE in 1 BOTTLE (0280-4095-60) |
Product NDC | 0280-4095 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | calcium carbonate |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20130315 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Bayer HealthCare LLC, Consumer Care |
Substance Name | CALCIUM CARBONATE |
Strength Number | 750 |
Strength Unit | mg/1 |
Pharmaceutical Classes |