Pain Relief
- Product NDC
- 21130-492
- 11-digit product format
- 211300492
- Labeler code
- 21130
- Product ID
- 21130-492_284fb7b3-5211-ebf1-e063-6394a90a0450
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- SAFEWAY
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-10
- Substance
- ACETAMINOPHEN
- Active strength
- 500 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
- Extra Strength
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-492-01 | Pain ReliefExtra Strength | 100 in 1 BOTTLE, PLASTIC | TABLET, COATED | 100 | | 3 |
| 21130-492-01 | Pain ReliefExtra Strength | 1 in 1 CARTON | TABLET, COATED | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21130-492 | PAIN RELIEF EXTRA STRENGTH (ACETAMINOPHEN) TABLET, COATED [SAFEWAY] | 3 | Current NDC, 2 package rows | 20241204_d2d15e06-e9eb-3d2b-e053-2995a90a1cec.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 21130-492-01 | 21130049201 | 1 BOTTLE, PLASTIC in 1 CARTON (21130-492-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC | 2022-06-10 | No | No | Historical |