Alka-Seltzer Gold
- Product NDC
- 0280-4100
- 11-digit product format
- 002804100
- Labeler code
- 0280
- Product ID
- 0280-4100_4526b3d0-3667-afe5-e063-6294a90af3ab
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alka-Seltzer Gold
- Dosage form
- TABLET, EFFERVESCENT
- Route
- ORAL
- Labeler
- Bayer HealthCare LLC.
- Application
- M001
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-11-19
- Substance
- CITRIC ACID MONOHYDRATE; POTASSIUM BICARBONATE; SODIUM BICARBONATE
- Active strength
- 1000; 344; 1050 mg/1; mg/1; mg/1
- Pharmacologic classes
- 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 Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Alka-Seltzer Gold
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| CITRIC ACID MONOHYDRATE | 1000 mg/1 |
| POTASSIUM BICARBONATE | 344 mg/1 |
| SODIUM BICARBONATE | 1050 mg/1 |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| 2968PHW8QP | Internal UNII lookup |
| HM5Z15LEBN | Internal UNII lookup |
| 8MDF5V39QO | Internal UNII lookup |
Harmonized RxCUI identifiers#
| Identifier | FDA.report destination |
|---|---|
| 1536474 | Internal RxNorm lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 0824bedb-413b-2fa0-e054-00144ff88e88 | Available on FDA.report |
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0280-4100-63 | Alka-Seltzer Gold | 18 in 1 CARTON | TABLET, EFFERVESCENT | 18 | 9 | |
| 0280-4100-63 | Alka-Seltzer Gold | 2 in 1 POUCH | TABLET, EFFERVESCENT | 2 | 9 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0280-4100-36 | EA - Each | 0280-4100 | b2530812-3cc3-45dd-95cc-04caf46a7586 | 1 | 2018-03-08 |
| 0280-4100-63 | EA - Each | 0280-4100 | e1b67ba6-d596-47b5-89fb-c8ebb74f9d5d | 1 | 2018-04-19 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| FEVIA Acid Control | CALCIUM CARBONATE | VIVUNT PHARMA LLC | 4b1bd2d1-c909-f5db-e063-6394a90a84bc | 2026-07-15 | Warnings | M001 |
| FEVIA Acid Control | CALCIUM CARBONATE | VIVUNT PHARMA LLC | 4d695a90-6502-3020-e063-6394a90ab0c3 | 2026-07-15 | Warnings | M001 |
| GOOD NEIGHBOR PHARMACY Antacid Extra Strength | ALUMINUM HYDROXIDE AND MAGNESIUM CARBONATE | Amerisource Bergen | 5e346dc0-69ce-4cc5-bb5d-bfa833e11c1f | 2026-07-13 | Warnings | M001 |
| Major Regular Strength Assorted Flavors | ANTACID TABLETS | Major Pharmaceuticals | 2ba0eeb2-7048-4259-83d5-9f4ec1c92d32 | 2026-07-13 | Warnings | M001 |
| Good Neighbor Extra Strength Assorted Fruits | CALCIUM CARBONATE | AMERISOURCE BERGEN | abf564a1-0823-433d-a023-8be4e085daf4 | 2026-07-13 | Warnings | M001 |
| Omeprazole, 24/7 Life by 7-Eleven | OMEPRAZOLE TABLET, DELAYED RELEASE | Lil' Drug Store Products, Inc. | 36d8a272-6cca-e759-e063-6394a90a9df8 | 2026-07-08 | Warnings | M001 |
| TUMS ULTRA | CALCIUM CARBONATE | Haleon US Holdings LLC | f4786707-a0f7-4ba8-9656-06278d1b4b6c | 2026-07-07 | Warnings | M001 |
| Tums Ultra | CALCIUM CARBONATE | Haleon US Holdings LLC | c544120f-15f0-48b5-88b2-d4820f180f50 | 2026-07-07 | Warnings | M001 |
| Regular Strength Assorted Flavors | ANTACID CALCIUM CARBONATE | AKRON PHARMA INC | 3f7fe022-aee9-b899-e063-6394a90afb4e | 2026-07-07 | Warnings | M001 |
| Magnesium Oxide | MAGNESIUM OXIDE | Westminster Pharmaceuticals, LLC | 52eeac0e-94bb-48c3-81dc-578e96406c01 | 2026-07-06 | Warnings | M001 |
| Kids Tummy Relief | CALCIUM CARBONATE | PNP Pharmaceuticals Inc. | 5103a317-5c4a-ec96-e063-6294a90aad7e | 2026-07-01 | Warnings | M001 |
| Rolaids MAX STRENGTH 1500 | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | THE PROCTER & GAMBLE MANUFACTURING COMPANY | 47f5a78b-66b6-2e09-e063-6294a90a8ad5 | 2026-07-01 | Warnings | M001 |
| Childrens Antacid | CALCIUM CARBONATE | DOLGENCORP, LLC | 4d6ebc7e-ef39-47e8-91e9-f38484329fa9 | 2026-06-30 | Warnings | M001 |
| Ultra Strength Antacid | CALCIUM CARBONATE CHEWABLE TABLETS | CVS Pharmacy. Inc. | 24cec2bc-cf12-b513-e063-6394a90a9447 | 2026-06-30 | Warnings | M001 |
| Childrens Stomach Relief | CALCIUM CARBONATE | Chain Drug Marketing Association, Inc. | fb47d693-72d7-4586-9855-5e833ad1406f | 2026-06-18 | Warnings | M001 |
| Dr. Sana Alivio Digestivo UPSET STOMACH | EFEFERVESCENT ANTACID | EVI LABS | 51b8750c-3fcf-2543-e063-6394a90a7a8f | 2026-06-16 | Warnings | M001 |
| E-Z-GAS II | ANTACID/ANTIFLATULENT | E-Z-EM, INC. | 4e12e1cb-b033-076d-e054-00144ff8d46c | 2026-06-15 | Warnings | M001 |
| Sodium Bicarbonate | SODIUM BICARBONATE | Cardinal Health 107, LLC | 60c2a176-8854-4479-b853-d07fe9a1830c | 2026-06-12 | Warnings | M001 |
| Mag-Al Plus | ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE, AND SIMETHICONE | Cardinal Health 107, LLC | 08df7403-9ee3-4a43-a151-c1a6ef7a7549 | 2026-06-10 | Warnings | M001 |
| Childrens Antacid | CALCIUM CARBONATE | Rite Aid Corporation | d09c2d99-9a1f-4eae-a048-ab6dbf74a798 | 2026-06-09 | Warnings | M001 |
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 1536474 | citric acid 1000 MG / potassium bicarbonate 344 MG / sodium bicarbonate 1050 MG Effervescent Oral Tablet | PSN | 0824bedb-413b-2fa0-e054-00144ff88e88 | 9 |
| 1536474 | citric acid 1000 MG / potassium bicarbonate 344 MG / sodium bicarbonate 1050 MG Effervescent Oral Tablet | SCD | 0824bedb-413b-2fa0-e054-00144ff88e88 | 9 |
| 1536474 | Citric Acid 1000 MG / K+ bicarbonate 344 MG / NaHCO3 1050 MG Effervescent Oral Tablet | SY | 0824bedb-413b-2fa0-e054-00144ff88e88 | 9 |
| 1536474 | Citric Acid 1000 MG / Pot bicarbonate 344 MG / NaHCO3 1050 MG Effervescent Oral Tablet | SY | 0824bedb-413b-2fa0-e054-00144ff88e88 | 9 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 0280-4100-63 | 00280410063 | 18 POUCH in 1 CARTON (0280-4100-63) / 2 TABLET, EFFERVESCENT in 1 POUCH | 18 pouch | 2014-11-19 | 0000-00-00 | No | No | Current |