Acetaminophen
- Product NDC
- 71205-730
- 11-digit product format
- 712050730
- Labeler code
- 71205
- Product ID
- 71205-730_8bf62cab-8919-4e74-84aa-dc987ca3f431
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-05-05
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71205-730-04 | 71205073004 | 118 mL in 1 BOTTLE, PLASTIC (71205-730-04) | 118 ml | 2022-12-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Acetaminophen | Proficient Rx LP | 2023-12-01 | HUMAN OTC DRUG LABEL | 2 |