Pain Reliever
- Product NDC
- 0363-0278
- 11-digit product format
- 003630278
- Labeler code
- 0363
- Product ID
- 0363-0278_9596606a-d83c-44a9-9cbf-89b27ed87e30
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Walgreens
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-01-31
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/15mL
- 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
- Brand name suffix
- Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/15mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307684 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0363-0278-08 | Pain RelieverExtra Strength | 237 mL in 1 BOTTLE, PLASTIC | LIQUID | 237 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0363-0278 | PAIN RELIEVER EXTRA STRENGTH (ACETAMINOPHEN) LIQUID [WALGREENS] | 6 | Current NDC, Legacy NDC, 1 package rows | 20231010_b4b06d32-6a09-4c43-980b-377b617ba739.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 |
|---|
| 0363-0278-08 | 00363027808 | 237 mL in 1 BOTTLE, PLASTIC (0363-0278-08) | 237 ml | 2016-01-31 | 0000-00-00 | No | No | Current |