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NDC 00280-0047-36 Alka-Seltzer Heartburn 1000; 1940 mg/1; mg/1 Details
Alka-Seltzer Heartburn 1000; 1940 mg/1; mg/1
Alka-Seltzer Heartburn 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; SODIUM BICARBONATE.
Product Information
NDC | 00280-0047 |
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Product ID | 0280-0047_0bb521d3-b3bc-f576-e063-6294a90a3a18 |
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 Heartburn |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | Anhydrous citric acid, Sodium bicarbonate (heat-treated) |
Product Type | HUMAN OTC DRUG |
Dosage Form | TABLET, EFFERVESCENT |
Route | ORAL |
Active Ingredient Strength | 1000; 1940 |
Active Ingredient Units | mg/1; mg/1 |
Substance Name | CITRIC ACID MONOHYDRATE; 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], Inhibition Large Intestine Fluid/Electrolyte Absorpti |
DEA Schedule | n/a |
Marketing Category | OTC MONOGRAPH DRUG |
Application Number | M001 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00280-0047-36 (00280004736)
NDC Package Code | 0280-0047-36 |
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Billing NDC | 00280004736 |
Package | 18 POUCH in 1 CARTON (0280-0047-36) / 2 TABLET, EFFERVESCENT in 1 POUCH |
Marketing Start Date | 2010-03-02 |
NDC Exclude Flag | N |
Pricing Information | N/A |