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NDC 00132-0107-24 Pedia-Lax 50 mg/15mL Details
Pedia-Lax 50 mg/15mL
Pedia-Lax is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by C.B. Fleet Company, Inc.. The primary component is DOCUSATE SODIUM.
MedlinePlus Drug Summary
Stool softeners are used on a short-term basis to relieve constipation by people who should avoid straining during bowel movements because of heart conditions, hemorrhoids, and other problems. They work by softening stools to make them easier to pass.
Related Packages: 00132-0107-24Last Updated: 03/24/2024
MedLinePlus Full Drug Details: Stool Softeners
Product Information
| NDC | 00132-0107 |
|---|---|
| Product ID | 0132-0107_25b30df6-095c-4ed1-b695-26a7b56b8da0 |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Pedia-Lax |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Docusate Sodium |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | mg/15mL |
| Substance Name | DOCUSATE SODIUM |
| Labeler Name | C.B. Fleet Company, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH NOT FINAL |
| Application Number | part334 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 00132-0107-24 (00132010724)
| NDC Package Code | 0132-0107-24 |
|---|---|
| Billing NDC | 00132010724 |
| Package | 118 mL in 1 CARTON (0132-0107-24) |
| Marketing Start Date | 2020-02-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |