Genexa Infants Pain and Fever
- Product NDC
- 69676-0042
- 11-digit product format
- 696760042
- Labeler code
- 69676
- Product ID
- 69676-0042_51588b9a-d5ac-4667-e063-6294a90a432c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Genexa Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-03-10
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Genexa Infants Pain and Fever
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307668 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69676-0042-9 | Genexa Infants Pain and Fever | 1 in 1 CARTON | SUSPENSION | 1 | | 8 |
| 69676-0042-9 | Genexa Infants Pain and Fever | 59 mL in 1 BOTTLE | SUSPENSION | 59 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69676-0042 | GENEXA INFANTS PAIN AND FEVER (ACETAMINOPHEN) SUSPENSION [GENEXA INC.] | 6 | Current NDC, Legacy NDC, 2 package rows | 20250406_c59cbf0e-1381-4dd2-e053-2a95a90a853a.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 |
|---|
| 69676-0042-9 | 69676004209 | 1 BOTTLE in 1 CARTON (69676-0042-9) / 59 mL in 1 BOTTLE | 1 bottle | 2025-03-10 | 0000-00-00 | No | No | Current |