NDC 50845-0102-1 - Stomach Distress
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 50845-0102
- Requested NDC
- 50845-0102-1
- Package NDCs from labels
- 50845-0102-1, 50845-0102-2
- Manufacturer
- Liddell Laboratories, Inc. | Apotheca Company
- Effective date
- 2021-09-16
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Stomach Distress - Liddell Laboratories, Inc. | Apotheca Company | Liddell Laboratories, Inc. | Apotheca Company | 2021-09-16 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0102-2 | 2021-09-16 | C162847 | 48780-1 | 9d75b9cf-fda0-f424-e053-dadaa90a57ce | Drug Facts: |
| 50845-0102-2 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-fda0-f424-e053-dadaa90a57ce | Drug Facts: |
DailyMed Socrata Ingredients#
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.
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| Bridged Ring Combination 9311 | BRIDGED RING COMBINATION | Professional Complementary Health Formulas | b4033f70-d974-493d-8ded-eaa3240bdac5 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
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| Carduus Combination 9215 | CARDUUS COMBINATION | Professional Complementary Health Formulas | a244de13-836f-49b5-8c7a-d45bde704d78 | 2026-01-08 | Warnings | S003A158SB |
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| Lumbar Drops 5013 | LUMBAR DROPS | Professional Complementary Health Formulas | ee6b54ea-fb6a-4723-8a0f-970aa82fea80 | 2026-01-08 | Warnings | ETJ7Z6XBU4 |
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| Simple Chlorinated Combination 9315 | SIMPLE CHLORINATED COMBINATION | Professional Complementary Health Formulas | c1ab9a34-8a22-4840-ab8b-ef666dca155a | 2026-01-08 | Warnings | 269XH13919 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.