United States · FDA National Drug Code directory
OCUFRESH
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
- 64108-313_b91fb96f-4fa4-462b-a8c5-c07d2eb9a42f
- Product NDC
- 64108-313
- Form
- LIQUID
- Composition / generic term
- Water
- Labeler
- Optics Laboratory Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20140115
- Source listing expiry
- 20261231
Source-listed ingredients
- WATER — .988 mL/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 mL in 1 BOTTLE (64108-313-01) · 64108-313-01
- 6 BOTTLE in 1 PACKAGE (64108-313-06) / 20 mL in 1 BOTTLE (64108-313-01) · 64108-313-06
- 24 BOTTLE in 1 PACKAGE (64108-313-24) / 20 mL in 1 BOTTLE (64108-313-01) · 64108-313-24
- 60 BOTTLE in 1 PACKAGE (64108-313-60) / 20 mL in 1 BOTTLE (64108-313-01) · 64108-313-60
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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