Pain Reliever
- Product NDC
- 66715-6871
- 11-digit product format
- 667156871
- Labeler code
- 66715
- Product ID
- 66715-6871_2969c6e6-7fee-195e-e063-6294a90a268f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen 500mg, film-coated caplet
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lil' Drug Store Products, Inc.
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-03-04
- Substance
- ACETAMINOPHEN
- Active strength
- 500 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 362O9ITL9D | ACETAMINOPHEN | 103-90-2 | ACETAMINOPHEN |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 66715-6871-4 | 66715687104 | 1 BOTTLE, PLASTIC in 1 CARTON (66715-6871-4) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC | 2022-03-04 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Pain Reliever | Lil' Drug Store Products, Inc. | 2024-12-16 | HUMAN OTC DRUG LABEL | 3 |