Childrens Tukol Acetaminophen Fever Reducer Pain Reducer
- Product NDC
- 50066-525
- 11-digit product format
- 500660525
- Labeler code
- 50066
- Product ID
- 50066-525_abbc3017-0f3f-4c00-aa6f-c5786b17b423
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Genomma Lab USA, Inc.
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2016-05-03
- 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
- Childrens Tukol Acetaminophen Fever Reducer Pain Reducer
- 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 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50066-525-24 | Childrens Tukol Acetaminophen Fever Reducer Pain Reducer | 118 mL in 1 BOTTLE | LIQUID | 118 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50066-525 | CHILDRENS TUKOL ACETAMINOPHEN FEVER REDUCER PAIN REDUCER (ACETAMINOPHEN) LIQUID [GENOMMA LAB USA, INC.] | 1 | Current NDC, Legacy NDC, 1 package rows | 20170415_0540111a-fcde-492d-9ed5-bbd714b2acf0.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 |
|---|
| 50066-525-24 | 50066052524 | 118 mL in 1 BOTTLE (50066-525-24) | 118 ml | 2016-05-03 | 0000-00-00 | No | No | Current |