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 |
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| 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 |