Kids Pain and Fever
- Product NDC
- 69676-0089
- 11-digit product format
- 696760089
- Labeler code
- 69676
- Product ID
- 69676-0089_35d00d8c-b098-0878-e063-6294a90a5af9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Genexa Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-03-13
- 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
- Kids Pain and Fever
- 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 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69676-0089-9 | Kids Pain and Fever | 118 mL in 1 BOTTLE, PLASTIC | LIQUID | 118 | | 2 |
| 69676-0089-9 | Kids Pain and Fever | 2 in 1 CARTON | LIQUID | 2 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69676-0089 | KIDS PAIN AND FEVER (ACETAMINOPHEN) LIQUID [GENEXA INC.] | 2 | Current NDC, 2 package rows | 20250525_fcffa7e6-145c-6bc0-e053-6294a90a4751.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 69676-0089-9 | 69676008909 | 2 BOTTLE, PLASTIC in 1 CARTON (69676-0089-9) / 118 mL in 1 BOTTLE, PLASTIC | 2025-03-13 | No | No | Current |