Pain Relief
- Product NDC
- 63868-175
- 11-digit product format
- 638680175
- Labeler code
- 63868
- Product ID
- 63868-175_9b26e025-90a0-430c-8cef-bb8439892194
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- QUALITY CHOICE (Chain Drug Marketing Association)
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-10-31
- Substance
- ACETAMINOPHEN
- Active strength
- 160 mg/5mL
- 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
- Childrens
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ACETAMINOPHEN | 160 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 362O9ITL9D |
| Rxcui | 307668 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63868-175-26 | Pain ReliefChildrens | 118 mL in 1 BOTTLE | SUSPENSION | 118 | | 5 |
| 63868-175-26 | Pain ReliefChildrens | 1 in 1 BOX | SUSPENSION | 1 | | 5 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63868-175 | PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)] | 5 | Current NDC, Legacy NDC, 2 package rows | 20241212_223ffb2b-3ee5-4118-955b-bc4fa4e8a2e6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63868-175-26 | 63868017526 | 1 BOTTLE in 1 BOX (63868-175-26) / 118 mL in 1 BOTTLE | 1 bottle | 2015-10-31 | 2021-12-30 | No | No | Current |