Pain Relief
- Product NDC
- 49035-278
- 11-digit product format
- 490350278
- Labeler code
- 49035
- Product ID
- 49035-278_a330c12d-8917-4ed3-a758-735577f8c68b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-12-31
- 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 Relief
- 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 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 49035-278-08 | Pain ReliefExtra 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 |
|---|
| 49035-278 | PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) LIQUID [EQUATE (WAL-MART STORES, INC.) (SEE ALSO WAL-MART INC)] | 6 | Current NDC, Legacy NDC, 1 package rows | 20240321_872c5220-a379-4dc1-b99c-f11ebb82db35.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 |
|---|
| 49035-278-08 | 49035027808 | 237 mL in 1 BOTTLE, PLASTIC (49035-278-08) | 237 ml | 2015-12-31 | 0000-00-00 | No | No | Current |