Alka Seltzer Original is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Navajo Manufacturing Company Inc.. The primary component is Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate.
Product ID | 67751-143_3cf2c5bd-3b02-1bf5-e054-00144ff8d46c |
NDC | 67751-143 |
Product Type | Human Otc Drug |
Proprietary Name | Alka Seltzer Original |
Generic Name | Anhydrous Citric Acid, Aspirin, Sodium Bicarbonate |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2016-09-16 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part343 |
Labeler Name | Navajo Manufacturing Company Inc. |
Substance Name | ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE |
Active Ingredient Strength | 1000 mg/1; mg/1; mg/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2016-09-16 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-09-16 |
Marketing Category | OTC monograph not final |
Application Number | part343 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2016-09-16 |
Ingredient | Strength |
---|---|
ANHYDROUS CITRIC ACID | 1000 mg/1 |
SPL SET ID: | fbf52eee-b307-4640-8f90-909bebe54a42 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
Pharm Class PE | |
PHarm Class EPC | |
NUI Code |
NDC | Brand Name | Generic Name |
---|---|---|
67751-143 | Alka Seltzer Original | ANHYDROUS CITRIC ACID, ASPIRIN, SODIUM BICARBONATE |
73097-001 | Alka Seltzer Original | ANHYDROUS CITRIC ACID, ASPIRIN, SODIUM BICARBONATE |