pain relief
- Product NDC
- 37808-130
- 11-digit product format
- 378080130
- Labeler code
- 37808
- Product ID
- 37808-130_2b505669-63d4-4277-8cf6-bfb24a221592
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- H E B
- Application
- M013
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1996-04-29
- 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
- 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 |
|---|
| 37808-130-26 | pain relief | 1 in 1 CARTON | SUSPENSION | 1 | | 9 |
| 37808-130-26 | pain relief | 118 mL in 1 BOTTLE | SUSPENSION | 118 | | 9 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 37808-130 | PAIN RELIEF (ACETAMINOPHEN) SUSPENSION [H E B] | 9 | Current NDC, Legacy NDC, 2 package rows | 20240913_3258ef39-c36e-4a97-8631-89b8d4caf058.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 |
|---|
| 37808-130-26 | 37808013026 | 1 BOTTLE in 1 CARTON (37808-130-26) / 118 mL in 1 BOTTLE | 1 bottle | 1996-04-29 | 0000-00-00 | No | No | Current |