Pain Relief
- Product NDC
- 49580-0821
- 11-digit product format
- 495800821
- Labeler code
- 49580
- Product ID
- 49580-0821_fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-07-31
- 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 |
|---|
| 49580-0821-4 | Pain Relief | 1 in 1 BOX | SUSPENSION | 1 | | 2 |
| 49580-0821-4 | Pain Relief | 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 |
|---|
| 49580-0821 | PAIN RELIEF (ACETAMINOPHEN) SUSPENSION [P & L DEVELOPMENT, LLC] | 2 | Current NDC, 2 package rows | 20240731_1c081a7c-8cff-4253-97ac-5fa74a5c0668.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 49580-0821-4 | 49580082104 | 1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4) / 118 mL in 1 BOTTLE, PLASTIC | 2024-07-31 | No | No | Current |