Childrens Acetaminophen
- Product NDC
- 71335-2722
- 11-digit product format
- 713352722
- Labeler code
- 71335
- Product ID
- 71335-2722_e7fdf4db-c5e3-433a-8e94-13f5c25ca933
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-04-09
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 71335-2722_e7fdf4db-c5e3-433a-8e94-13f5c25ca933
- SPL ID
- e7fdf4db-c5e3-433a-8e94-13f5c25ca933
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- Childrens Acetaminophen
- Generic name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Marketing start
- 2014-04-09
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M013
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307668 |
| Spl Set Id | 190bb2dc-92b4-4b59-a47f-a0251df8261c |
| Manufacturer Name | Bryant Ranch Prepack |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 71335-2722-1 | 1 BOTTLE in 1 CARTON (71335-2722-1) / 118 mL in 1 BOTTLE | 2025-07-29 | No |
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 |
|---|
| 71335-2722-1 | 71335272201 | 1 BOTTLE in 1 CARTON (71335-2722-1) / 118 mL in 1 BOTTLE | 1 bottle | 2025-07-29 | No | No | Historical |