Mucinex Childrens
- Product NDC
- 72854-062
- 11-digit product format
- 728540062
- Labeler code
- 72854
- Product ID
- 72854-062_52564ca6-63f6-f1ae-e063-6294a90a33df
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Dextromethorphan HBr, Triprolidine HCl
- Dosage form
- KIT
- Route
- ORAL
- Labeler
- Reckitt Benckiser LLC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-06-01
- 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
- Mucinex Childrens
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 4cee80e5-e412-e832-e063-6394a90aeb90 | Available on FDA.report |
DailyMed Product Concepts#
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 |
|---|---|---|---|---|---|---|---|
| 72854-062-04 | 72854006204 | 2 BOTTLE in 1 CARTON (72854-062-04) / 1 KIT in 1 BOTTLE * 118 mL in 1 BOTTLE * 118 mL in 1 BOTTLE | 2 bottle | 2026-06-01 | No | No | Current |