Pain Relief Fever Reducer
- Product NDC
- 80272-002
- Requested package NDC
- 80272-002-04
- 11-digit product format
- 802720002
- Labeler code
- 80272
- Product ID
- 80272-002_10e22b9b-a5c6-4ede-9928-ae885a87eb8e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Ellywell, LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-09-30
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 80272-002-04 | Pain Relief Fever Reducerchildren | 1 in 1 BOX | SUSPENSION | 1 | | 6 |
| 80272-002-04 | Pain Relief Fever Reducerchildren | 118 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 118 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 80272-002 | PAIN RELIEF FEVER REDUCER CHILDREN (ACETAMINOPHEN) SUSPENSION [ELLYWELL, LLC] | 6 | Legacy NDC, 2 package rows | 20241016_92f26bb4-da58-4db4-83bc-aec1ebab2dbf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 80272-002-04 | 80272000204 | 1 BOTTLE, PLASTIC in 1 BOX (80272-002-04) > 118 mL in 1 BOTTLE, PLASTIC | 2020-09-30 | 0000-00-00 | No | No | Current |