Alka Seltzer Original
- Product NDC
- 67751-143
- Requested package NDC
- 67751-143-01
- 11-digit product format
- 677510143
- Labeler code
- 67751
- Product ID
- 67751-143_e5464c88-a96d-77d2-e053-2995a90a8bc0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ANHYDROUS CITRIC ACID, ASPIRIN, SODIUM BICARBONATE
- Dosage form
- TABLET, EFFERVESCENT
- Route
- ORAL
- Labeler
- Navajo Manufacturing Company Inc.
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-09-16
- Marketing end
- 0000-00-00
- Substance
- ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE
- Active strength
- 1000 mg/1; mg/1; mg/1
- Pharmacologic classes
- Acidifying Activity [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Cyclooxygenase Inhibitors [MoA], Decreased Coagulation Factor Activity [PE], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Platelet Aggregation Inhibitor [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 67751-143 | 67751-143-01 | D | Discontinued by firm | 2026-10-12 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | excluded package | package | 67751-143 | 67751-143-01 | D | Discontinued by firm | excluded / ndc_excluded.zip | d630ba8d3edf… | 732f749b63fb… | |
| 2025-08-27 00:01 UTC · source 2025-08-26 | excluded package | package | 67751-143 | 67751-143-01 | D | Discontinued by firm | excluded / ndc_excluded.zip | f5e01cc5f278… | a2eaf40c39c3… |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 67751-143-01 | 67751014301 | 1 POUCH in 1 CARTON (67751-143-01) > 2 TABLET, EFFERVESCENT in 1 POUCH | 1 pouch | 2016-09-16 | 0000-00-00 | No | No | Current |