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NDC 00280-4100-63 Alka-Seltzer Gold 1000; 344; 1050 mg/1; mg/1; mg/1 Details
Alka-Seltzer Gold 1000; 344; 1050 mg/1; mg/1; mg/1
Alka-Seltzer Gold is a ORAL TABLET, EFFERVESCENT in the HUMAN OTC DRUG category. It is labeled and distributed by Bayer HealthCare LLC.. The primary component is CITRIC ACID MONOHYDRATE; POTASSIUM BICARBONATE; SODIUM BICARBONATE.
Product Information
NDC | 00280-4100 |
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Product ID | 0280-4100_0bb5329c-888f-9e66-e063-6394a90a3b9e |
Associated GPIs | |
GCN Sequence Number | n/a |
GCN Sequence Number Description | n/a |
HIC3 | n/a |
HIC3 Description | n/a |
GCN | n/a |
HICL Sequence Number | n/a |
HICL Sequence Number Description | n/a |
Brand/Generic | n/a |
Proprietary Name | Alka-Seltzer Gold |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Alka-Seltzer Gold |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, EFFERVESCENT |
Route | ORAL |
Active Ingredient Strength | 1000; 344; 1050 |
Active Ingredient Units | mg/1; mg/1; mg/1 |
Substance Name | CITRIC ACID MONOHYDRATE; POTASSIUM BICARBONATE; SODIUM BICARBONATE |
Labeler Name | Bayer HealthCare LLC. |
Pharmaceutical Class | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH DRUG |
Application Number | M001 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00280-4100-63 (00280410063)
NDC Package Code | 0280-4100-63 |
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Billing NDC | 00280410063 |
Package | 18 POUCH in 1 CARTON (0280-4100-63) / 2 TABLET, EFFERVESCENT in 1 POUCH |
Marketing Start Date | 2014-11-19 |
NDC Exclude Flag | N |
Pricing Information | N/A |