Pain Reliever
- Product NDC
- 79903-172
- 11-digit product format
- 799030172
- Labeler code
- 79903
- Product ID
- 79903-172_4cfa7932-bb16-4e51-8d30-995a7f3e20f3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- WALMART INC. (see also Equate)
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-12-30
- 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
- Pain Reliever
- 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 Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79903-172-04 | Pain Reliever | 1 in 1 BOX | SUSPENSION | 1 | | 2 |
| 79903-172-04 | Pain Reliever | 118 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 118 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79903-172 | PAIN RELIEVER (ACETAMINOPHEN) SUSPENSION [WALMART INC. (SEE ALSO EQUATE)] | 2 | Current NDC, Legacy NDC, 2 package rows | 20240627_7d86a03f-74f4-4b24-b6a6-8747acfe905e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79903-172-04 | 79903017204 | 1 BOTTLE, PLASTIC in 1 BOX (79903-172-04) / 118 mL in 1 BOTTLE, PLASTIC | 2022-12-30 | 0000-00-00 | No | No | Current |