pain relief
- Product NDC
- 79481-0045
- 11-digit product format
- 794810045
- Labeler code
- 79481
- Product ID
- 79481-0045_05b99fa2-df58-4354-b1b8-78d87781bd95
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Meijer Distribution, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-04-14
- Substance
- ACETAMINOPHEN
- Active strength
- 1000 mg/30mL
- 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
- Brand name suffix
- EXTRA STRENGTH
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 1000 mg/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307684 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 79481-0045-1 | pain reliefEXTRA STRENGTH | 237 mL in 1 BOTTLE, PLASTIC | SOLUTION | 237 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79481-0045 | PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) SOLUTION [MEIJER DISTRIBUTION, INC.] | 6 | Current NDC, Legacy NDC, 1 package rows | 20241108_ae84eb7e-a70b-4311-b2dc-ad153047a516.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 |
|---|
| 79481-0045-1 | 79481004501 | 237 mL in 1 BOTTLE, PLASTIC (79481-0045-1) | 237 ml | 2021-04-14 | 0000-00-00 | No | No | Current |