Rompe Pechito EX for Kids
- Product NDC
- 58593-007
- 11-digit product format
- 585930007
- Labeler code
- 58593
- Product ID
- 58593-007_5b79b476-1c9a-3e65-e063-6294a90a4f0c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Guaifenesin
- Dosage form
- SYRUP
- Route
- ORAL
- Labeler
- Efficient Laboratories, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-01
- Substance
- GUAIFENESIN
- Active strength
- 50 mg/2.5mL
- Pharmacologic classes
- Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [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
- Rompe Pechito EX for Kids
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| GUAIFENESIN | 50 mg/2.5mL |
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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 58593-007-04 | 58593000704 | 1 BOTTLE in 1 CARTON (58593-007-04) / 118 mL in 1 BOTTLE | 1 bottle | 2026-09-01 | No | No | Current |