CLEARLAX
- Product NDC
- 21130-637
- 11-digit product format
- 211300637
- Labeler code
- 21130
- Product ID
- 21130-637_9276dc8e-612f-428c-9ed4-780fd33eded5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Polyethylene Glycol 3350
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Safeway
- Application
- ANDA090685
- Marketing category
- ANDA
- Marketing start
- 2026-03-06
- Substance
- POLYETHYLENE GLYCOL 3350
- Active strength
- 17 g/17g
- Pharmacologic classes
- Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- CLEARLAX
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POLYETHYLENE GLYCOL 3350 | 17 g/17g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G2M7P15E5P |
| Rxcui | 876193, 880407 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21130-637-02 | CLEARLAX | 238 g in 1 BOTTLE | POWDER, FOR SOLUTION | 238 | | 3 |
| 21130-637-09 | CLEARLAX | 765 g in 1 BOTTLE | POWDER, FOR SOLUTION | 765 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 21130-637-02 | 21130063702 | 238 g in 1 BOTTLE (21130-637-02) | 238 g | 2026-03-06 | No | No | Current |
| 21130-637-09 | 21130063709 | 765 g in 1 BOTTLE (21130-637-09) | 765 g | 2026-05-01 | 0 | | Current |