TYLENOL For Children Plus Adults
- Product NDC
- 50580-177
- 11-digit product format
- 505800177
- Labeler code
- 50580
- Product ID
- 50580-177_35a3c165-116d-b171-e063-6394a90a8abd
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Kenvue Brands LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-07-01
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- TYLENOL For Children Plus Adults
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307668, 828555 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50580-177-08 | TYLENOL For Children Plus Adults | 240 mL in 1 BOTTLE | SUSPENSION | 240 | | 5 |
| 50580-177-08 | TYLENOL For Children Plus Adults | 1 in 1 CARTON | SUSPENSION | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50580-177 | TYLENOL FOR CHILDREN PLUS ADULTS (ACETAMINOPHEN) SUSPENSION [KENVUE BRANDS LLC] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250523_5bb8ef99-a94b-49f9-89f9-cd1ce0a47a42.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50580-177-08 | 50580017708 | 1 BOTTLE in 1 CARTON (50580-177-08) / 240 mL in 1 BOTTLE | 1 bottle | 2021-07-01 | 0000-00-00 | No | No | Current |