Pain Reliever
- Product NDC
- 49580-2880
- 11-digit product format
- 495802880
- Labeler code
- 49580
- Product ID
- 49580-2880_7dfcadc9-97a1-4d12-b8d9-2053c4ee9273
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-15
- Marketing end
- 2026-12-30
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 49580-2880-4 | 49580288004 | 1 BOTTLE, PLASTIC in 1 BOX (49580-2880-4) / 118 mL in 1 BOTTLE, PLASTIC | 2024-03-15 | 2026-12-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Drug Facts | P & L Development, LLC | 2025-09-08 | HUMAN OTC DRUG LABEL | 4 |