PAIN RELIEF
- Product NDC
- 79481-0302
- 11-digit product format
- 794810302
- Labeler code
- 79481
- Product ID
- 79481-0302_09e4aea0-f446-457e-ab21-d0589db5d78f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Meijer, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-06-21
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 79481-0302_047c3a4a-e08c-428e-9943-a7da4f2c3f9a
- SPL ID
- 047c3a4a-e08c-428e-9943-a7da4f2c3f9a
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- PAIN RELIEF
- Generic name
- acetaminophen
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing start
- 2024-06-21
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- M013
- Listing expiration
- 2027-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 198440 |
| Spl Set Id | 1319bab8-8f17-44fb-9d91-099b0ba38a8d |
| Manufacturer Name | Meijer, Inc. |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 79481-0302-1 | 1 BOTTLE in 1 CARTON (79481-0302-1) / 100 TABLET, FILM COATED in 1 BOTTLE | 2024-06-21 | No |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 79481-0302-1 | 79481030201 | 1 BOTTLE in 1 CARTON (79481-0302-1) / 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2024-06-21 | No | No | Historical |