gas relief
- Product NDC
- 69452-581
- Requested package NDC
- 69452-581-24
- 11-digit product format
- 694520581
- Labeler code
- 69452
- Product ID
- 69452-581_5cb306dc-0f70-bf9e-e063-6294a90acb26
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- simethicone
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- BIONPHARMA INC.
- Application
- M002
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-30
- Substance
- DIMETHICONE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Skin Barrier Activity [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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
- gas relief
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| DIMETHICONE | 500 mg/1 |
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.
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 69452-581-24 | 69452058124 | 150 CAPSULE, LIQUID FILLED in 1 BOTTLE (69452-581-24) | 2026-09-30 | No | No | Current |