REFRESH LIQUIGEL

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 · 0

No packs registered.

Annotations

UNII (FDA Substance ID)

K679OBS311

CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED

RxCUI 491498

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "K679OBS311",
    "rxcui": "491498",
    "inchikey": null,
    "display_name": "CARBOXYMETHYLCELLULOSE SODIUM, 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": "0023-9205_772b77fa-d196-4a2b-a05a-ad1fe58d5985",
  "productndc": "0023-9205",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED",
  "proprietary_name": "REFRESH LIQUIGEL",
  "active_ingred_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Carboxymethylcellulose sodium",
  "start_marketing_date": "20011004",
  "active_numerator_strength": "10"
}

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