Pain Relief PM
- Product NDC
- 42507-095
- 11-digit product format
- 425070095
- Labeler code
- 42507
- Product ID
- 42507-095_440cb853-1454-0cda-e063-6294a90a73a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen and Diphenhydramine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- HYVEE INC
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-22
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500; 25 mg/1; mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- 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 PM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 500 mg/1 |
| DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D, TC2D6JAD40 |
| Rxcui | 1092189 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 42507-095-03 | Pain Relief PM | 1 in 1 CARTON | TABLET, COATED | 1 | | 3 |
| 42507-095-03 | Pain Relief PM | 100 in 1 BOTTLE, PLASTIC | TABLET, COATED | 100 | | 3 |
| 42507-095-17 | Pain Relief PM | 225 in 1 BOTTLE, PLASTIC | TABLET, COATED | 225 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 42507-095-03 | 42507009503 | 1 BOTTLE, PLASTIC in 1 CARTON (42507-095-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC | 2025-10-22 | No | No | Historical |
| 42507-095-17 | 42507009517 | 225 TABLET, COATED in 1 BOTTLE, PLASTIC (42507-095-17) | 2025-11-20 | No | No | Historical |