Pain Reliever
- Product NDC
- 49580-3278
- 11-digit product format
- 495803278
- Labeler code
- 49580
- Product ID
- 49580-3278_034d49b7-a878-45b5-9572-2eb3dc9368a9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-11-29
- Marketing end
- 2026-08-28
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/15mL
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pain Reliever
- Brand name suffix
- Extra Strength
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/15mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307684 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49580-3278-8 | Pain RelieverExtra Strength | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49580-3278 | PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) LIQUID [P & L DEVELOPMENT, LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231014_061df1fd-173a-4bd1-9600-540ac0f3964d.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 |
|---|
| 49580-3278-8 | 49580327808 | 237 mL in 1 BOTTLE, PLASTIC (49580-3278-8) | 237 ml | 2019-11-29 | 2026-08-28 | No | No | Current |