REFRESH Classic

UNIISPL

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

Identification

ManufacturerAllergan, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
0023050601
30 VIAL, SINGLE-USE in 1 CARTON (0023-0506-01) / .4 mL in 1 VIAL, SINGLE-USE
ndc11
0023050650
50 VIAL, SINGLE-USE in 1 CARTON (0023-0506-50) / .4 mL in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

532B59J990

POLYVINYL ALCOHOL, UNSPECIFIED

RxCUI 8570

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "532B59J990",
    "rxcui": "8570",
    "inchikey": null,
    "display_name": "POLYVINYL ALCOHOL, UNSPECIFIED",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "OPHTHALMIC",
  "spl_meta": {
    "31bf1d6c-9719-4060-b6a3-409a2fe7b560": {
      "match": "brand_token",
      "title": "REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.]",
      "spl_version": "11",
      "published_date": "2026-05-21"
    }
  },
  "productid": "0023-0506_2481e2c0-dbd8-4cbf-a545-057c522b6b5c",
  "productndc": "0023-0506",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "POLYVINYL ALCOHOL, UNSPECIFIED; POVIDONE",
  "proprietary_name": "REFRESH Classic",
  "active_ingred_unit": "mg/mL; mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Polyvinyl Alcohol, Povidone",
  "start_marketing_date": "19850912",
  "active_numerator_strength": "14; 6"
}

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