Pain Relief
- Product NDC
- 83324-034
- 11-digit product format
- 833240034
- Labeler code
- 83324
- Product ID
- 83324-034_c0c22985-1026-4e4a-8422-7e96ab744c92
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-03-15
- 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 Relief
- 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 |
|---|
| 83324-034-04 | Pain Relief | 118 mL in 1 BOTTLE, PLASTIC | SUSPENSION | 118 | | 2 |
| 83324-034-04 | Pain Relief | 1 in 1 BOX | SUSPENSION | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 83324-034 | PAIN RELIEF (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)] | 2 | Current NDC, 2 package rows | 20240316_2cde052d-22a4-470f-8d6a-7c17061b8ac8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 83324-034-04 | 83324003404 | 1 BOTTLE, PLASTIC in 1 BOX (83324-034-04) / 118 mL in 1 BOTTLE, PLASTIC | 2024-03-15 | No | No | Current |