United States · FDA National Drug Code directory
GenRx Anti-Bacterial Gel
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
- 59088-299_23733118-0f3a-e4a8-e063-6394a90aa41e
- Product NDC
- 59088-299
- Form
- LIQUID
- Composition / generic term
- Alcohol
- Labeler
- PureTek Corporation
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20200318
- Source listing expiry
- 20261231
Source-listed ingredients
- ALCOHOL — 62 mL/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 118 mL in 1 BOTTLE, PUMP (59088-299-08) · 59088-299-08
- 500 mL in 1 BOTTLE, DISPENSING (59088-299-31) · 59088-299-31
- 710 mL in 1 BOTTLE, PUMP (59088-299-39) · 59088-299-39
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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