Extra Strength Pain Reliever
- Product NDC
- 62936-0222
- 11-digit product format
- 629360222
- Labeler code
- 62936
- Product ID
- 62936-0222_115d0b60-84e9-7a34-e063-6394a90ae78c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- INGLES MARKETS, INC.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-01
- 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
- Extra Strength Pain Reliever
- 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 Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62936-0222-1 | Extra Strength Pain Reliever | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 62936-0222-5 | Extra Strength Pain Reliever | 50 in 1 BOTTLE | TABLET | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62936-0222 | EXTRA STRENGTH PAIN RELIEVER (ACETAMINOPHEN) TABLET [INGLES MARKETS, INC.] | 1 | Current NDC, 2 package rows | 20240216_115d0b4f-6f0f-79a9-e063-6394a90ab18a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62936-0222-1 | 62936022201 | 100 TABLET in 1 BOTTLE (62936-0222-1) | 100 tablet | 2019-09-01 | No | No | Historical |
| 62936-0222-5 | 62936022205 | 50 TABLET in 1 BOTTLE (62936-0222-5) | 50 tablet | 2019-09-01 | No | No | Historical |