United States · FDA National Drug Code directory
clearlax
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 59640-797_7a653744-4743-42bc-bc05-195a8abee466
- Product NDC
- 59640-797
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Polyethylene Glycol 3350
- Labeler
- H E B
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230117
- Source listing expiry
- 20261231
Source-listed ingredients
- POLYETHYLENE GLYCOL 3350 — 17 g/17g
These values do not establish equivalence or a dose recommendation.
Packages
- 238 g in 1 BOTTLE (59640-797-02) · 59640-797-02
- 510 g in 1 BOTTLE (59640-797-03) · 59640-797-03
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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