childrens acetaminophen
- Product NDC
- 71205-406
- Requested package NDC
- 71205-406-04
- 11-digit product format
- 712050406
- Labeler code
- 71205
- Product ID
- 71205-406_6ed1bf37-7a09-4b1e-8190-043bacf12429
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-04-09
- 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71205-406 | CHILDRENS ACETAMINOPHEN (ACETAMINOPHEN) SUSPENSION [PROFICIENT RX LP] | 4 | Legacy NDC | 20240223_35ec3a0e-0776-4d04-935f-96ad4fbb6d3a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-406-04 | 71205040604 | 1 BOTTLE in 1 CARTON (71205-406-04) > 118 mL in 1 BOTTLE | 1 bottle | 2020-02-19 | 0000-00-00 | No | No | Current |