OCUFRESH

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerOptics Laboratory Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
6410831301
20 mL in 1 BOTTLE (64108-313-01)
ndc11
6410831306
6 BOTTLE in 1 PACKAGE (64108-313-06) / 20 mL in 1 BOTTLE (64108-313-01)
ndc11
6410831324
24 BOTTLE in 1 PACKAGE (64108-313-24) / 20 mL in 1 BOTTLE (64108-313-01)
ndc11
6410831360
60 BOTTLE in 1 PACKAGE (64108-313-60) / 20 mL in 1 BOTTLE (64108-313-01)

Annotations

UNII (FDA Substance ID)

059QF0KO0R

WATER

RxCUI 11295

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "059QF0KO0R",
    "rxcui": "11295",
    "inchikey": "XLYOFNOQVPJJNP-UHFFFAOYSA-N",
    "display_name": "WATER",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "OPHTHALMIC",
  "spl_meta": {
    "b8e477a9-66b9-496b-92fb-3d4bbd7b36b5": {
      "match": "brand_token",
      "title": "OCUFRESH (WATER) LIQUID [OPTICS LABORATORY INC.]",
      "spl_version": "11",
      "published_date": "2025-12-31"
    }
  },
  "productid": "64108-313_b91fb96f-4fa4-462b-a8c5-c07d2eb9a42f",
  "productndc": "64108-313",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "WATER",
  "proprietary_name": "OCUFRESH",
  "active_ingred_unit": "mL/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Water",
  "start_marketing_date": "20140115",
  "active_numerator_strength": ".988"
}

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