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NDC 71399-0039-06 OneLAX 50 mg/5mL Details
OneLAX 50 mg/5mL
OneLAX is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Akron Pharma. 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: 71399-0039-06Last Updated: 05/19/2024
MedLinePlus Full Drug Details: Stool Softeners
Product Information
| NDC | 71399-0039 |
|---|---|
| Product ID | 71399-0039_63dcff8d-8254-450b-b3d0-e28425784eae |
| Associated GPIs | |
| GCN Sequence Number | 003017 |
| GCN Sequence Number Description | docusate sodium LIQUID 50 MG/5 ML ORAL |
| HIC3 | D6S |
| HIC3 Description | LAXATIVES AND CATHARTICS |
| GCN | 09131 |
| HICL Sequence Number | 001326 |
| HICL Sequence Number Description | DOCUSATE SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | OneLAX |
| 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/5mL |
| Substance Name | DOCUSATE SODIUM |
| Labeler Name | Akron Pharma |
| 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 71399-0039-06 (71399003906)
| NDC Package Code | 71399-0039-6 |
|---|---|
| Billing NDC | 71399003906 |
| Package | 473 mL in 1 BOTTLE (71399-0039-6) |
| Marketing Start Date | 2023-08-04 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |