EXTRA STRENGTH PAIN RELEIF
- Product NDC
- 70677-1242
- 11-digit product format
- 706771242
- Labeler code
- 70677
- Product ID
- 70677-1242_498af382-ead9-9b5d-e063-6294a90a7852
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Strategic Sourcing Services, LLC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-02-02
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- EXTRA STRENGTH PAIN RELEIF
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70677-1242-1 | EXTRA STRENGTH PAIN RELEIF | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70677-1242 | EXTRA STRENGTH PAIN RELEIF (ACETAMINOPHEN) TABLET, FILM COATED [STRATEGIC SOURCING SERVICES, LLC] | 2 | Current NDC, 1 package rows | 20250101_0392db17-c4f3-424b-9dee-549fc5df61c5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70677-1242-1 | 70677124201 | 120 TABLET, FILM COATED in 1 BOTTLE (70677-1242-1) | 2024-02-02 | No | No | Historical |