Pain Relief
- Product NDC
- 36800-900
- 11-digit product format
- 368000900
- Labeler code
- 36800
- Product ID
- 36800-900_28509d5e-d547-86f1-e063-6394a90a4425
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TopCo Associates LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2011-08-30
- Substance
- ACETAMINOPHEN
- Active strength
- 325 mg/1
- 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
- Regular Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 325 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 313782 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-900-02 | Pain ReliefRegular Strength | 100 in 1 BOTTLE, PLASTIC | TABLET | 100 | | 4 |
| 36800-900-02 | Pain ReliefRegular Strength | 1 in 1 CARTON | TABLET | 1 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-900 | PAIN RELIEF REGULAR STRENGTH (ACETAMINOPHEN) TABLET [TOPCO ASSOCIATES LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241204_c2d33352-431c-4683-a4fa-a54437e7b8d2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 36800-900-02 | 36800090002 | 1 BOTTLE, PLASTIC in 1 CARTON (36800-900-02) / 100 TABLET in 1 BOTTLE, PLASTIC | 2011-08-30 | 0000-00-00 | No | No | Current |