Over-the-counter drug · OTC MONOGRAPH DRUG
Alka-Seltzer Original NDC 0280-4000
anhydrous citric acid, aspirin, and sodium bicarbonate · Anhydrous citric acid 1000 mg/1 + 2 more ingredients · Tablet, Effervescent · Oral · Bayer HealthCare LLC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0280-4000-01 | 00280400001 | 6 POUCH in 1 CARTON (0280-4000-01) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Oct 10, 2012 | |
| 0280-4000-02 | 00280400002 | 24 POUCH in 1 CARTON (0280-4000-02) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Oct 10, 2012 | |
| 0280-4000-03 | 00280400003 | 18 POUCH in 1 CARTON (0280-4000-03) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Oct 10, 2012 | |
| 0280-4000-04 | 00280400004 | 58 POUCH in 1 CARTON (0280-4000-04) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Oct 10, 2012 | |
| 0280-4000-05 | 00280400005 | 36 POUCH in 1 CARTON (0280-4000-05) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Oct 10, 2012 | |
| 0280-4000-06 | 00280400006 | 12 POUCH in 1 CARTON (0280-4000-06) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Mar 24, 2022 | |
| 0280-4000-07 | 00280400007 | 26 POUCH in 1 CARTON (0280-4000-07) / 2 TABLET, EFFERVESCENT in 1 POUCHMarketed from Oct 10, 2012 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Alka-Seltzer Original
- Generic name (nonproprietary)
- anhydrous citric acid, aspirin, and sodium bicarbonate
- Active ingredients
- Anhydrous citric acid — 1000 mg/1Aspirin — 325 mg/1Sodium bicarbonate — 1916 mg/1
- Dosage form
- Tablet, Effervescent
- Route
- Oral
- Labeler
- Bayer HealthCare LLC.NDC labeler code 0280
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 013
- Marketing start
- Listing expires
- Other FDA classes
- Acidifying Activity (Mechanism)Alkalinizing Activity (Mechanism)Non-Steroidal (Chemical structure)Calcium Chelating Activity (Mechanism)Cyclooxygenase Inhibitors (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)Decreased Platelet Aggregation (Physiologic effect)Decreased Prostaglandin Production (Physiologic effect)
- Identifiers
- Product ID 0280-4000_4526b5f2-3b6b-b295-e063-6294a90ae6c1SPL ID 4526b5f2-3b6b-b295-e063-6294a90ae6c1SPL set ID 5be36a7f-7d1f-468d-9c29-92c8cd3ef1bcRxCUI 1536675, 1536680UNII XF417D3PSL, R16CO5Y76E, 8MDF5V39QO
- Pharmacologic class
- Anti-coagulant; Calculi Dissolution Agent; Nonsteroidal Anti-inflammatory Drug; Platelet Aggregation Inhibitor
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N400280400001followed by a unit qualifier and the quantityPackage 00280-4000-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses for the temporary relief of: heartburn, acid indigestion, and sour stomach when accompanied with headache or body aches and pains upset stomach with headache from overindulgence in food or drink headache, body aches, and pain alone
Excerpt only. Read the full label for complete information.
About NDC 0280-4000
- What is NDC 0280-4000?
- 0280-4000 is the product NDC for Alka-Seltzer Original, Anhydrous citric acid 1000 mg/1 + 2 more ingredients tablet, effervescent, listed with the FDA by Bayer HealthCare LLC.. It has 7 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Alka-Seltzer Original (ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE).
- What is the active ingredient?
- Anhydrous citric acid, Aspirin, Sodium bicarbonate.
- Who is the labeler?
- Bayer HealthCare LLC., NDC labeler code 0280. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Alka-Seltzer Original?
- 2 other product NDCs are listed under this name. See all Alka-Seltzer Original NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Alka-Seltzer Original products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Alka-Seltzer Originalanhydrous citric acid, aspirin, and sodium bicarbonate | Aspirin 325 mg/1 + 2 more ingredients | Tablet, EffervescentOral | R J General Corporation | 70264-014 | 70264-0014-01 |
| Alka-Seltzer Originalanhydrous citric acid, aspirin, and sodium bicarbonate | Anhydrous citric acid 1000 mg/1 + 2 more ingredients | Tablet, EffervescentOral | Select Consumer Group | 85237-1829 | 85237-1829-0185237-1829-0285237-1829-03+3 more |
Other NDCs under M 013
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Acetaminophen and Diphenhydramine hydrochloride | Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1 | TabletOral | WALMART INC. | 79903-267 |
| Cabinet Pain Reliever and Fever Reducer Refill Acetaminophenacetaminophen | Acetaminophen 500 mg/1 | TabletOral | Cabinet Health P.B.C. | 82725-3027 |
| Topcare Aspirinaspirin | Aspirin 81 mg/1 | Tablet, ChewableOral | Topco Associates LLC | 36800-274 |
| CounterAct Painacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Melaleuca, Inc. | 54473-305 |
| Acetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Precision Dose, Inc. | 68094-042 |
| Aspirin Regular Strengthaspirin | Aspirin 325 mg/1 | Tablet, Delayed releaseOral | Rugby Laboratories | 0536-1232 |
| Childrens Pain and Feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | AptaPharma Inc. | 76281-526 |
| Acetaminophen Regular Strengthacetaminophen | Acetaminophen 325 mg/1 | TabletOral | Magno-Humphries, Inc. | 54257-720 |
| Duralgina Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | TabletOral | Menper Distributors, Inc. | 53145-830 |
| Best Choice Effervescent Antacid Pain Reliefaspirin, citric acid, sodium bicarbonate | Aspirin 325 mg/1 + 2 more ingredients | Tablet, EffervescentOral | Valu Merchandisers Company | 63941-421 |
| Pain Relief Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | MARC GLASSMAN, INC. | 68998-392 |
| Acetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Precision Dose, Inc. | 68094-038 |
| Acetaminophen | Acetaminophen 500 mg/1 | TabletOral | Trifecta Pharmaceuticals USA LLC | 69396-144 |
| MAPAP Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | CapsuleOral | Major Pharmaceuticals | 0904-1987 |
| aspirin | Aspirin 81 mg/1 | Tablet, ChewableOral | Meijer Distribution Inc | 41250-467 |
| Aspirin | Aspirin 325 mg/1 | Tablet, Film coatedOral | A-S Medication Solutions | 50090-6195 |
| Pain Reliever Extra Strengthacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | Wal-Mart Stores Inc | 49035-919 |
| Aspirin | Aspirin 325 mg/1 | Tablet, CoatedOral | TIME CAP LABS INC | 49483-011 |
| rapid release pain reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | Publix Super Markets Inc | 56062-650 |
| Back and Body Pain Reliefaspirin, caffeine | Aspirin 500 mg/1; Caffeine 32.5 mg/1 | Tablet, Film coatedOral | WinCo Foods, LLC | 67091-430 |
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