REFRESH PLUS

SPL

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 · 5

ndc11
0023040305
5 VIAL, SINGLE-USE in 1 CARTON (0023-0403-05) / .4 mL in 1 VIAL, SINGLE-USE
ndc11
0023040310
100 VIAL, SINGLE-USE in 1 CARTON (0023-0403-10) / .4 mL in 1 VIAL, SINGLE-USE
ndc11
0023040330
30 VIAL, SINGLE-USE in 1 CARTON (0023-0403-30) / .4 mL in 1 VIAL, SINGLE-USE
ndc11
0023040350
50 VIAL, SINGLE-USE in 1 CARTON (0023-0403-50) / .4 mL in 1 VIAL, SINGLE-USE
ndc11
0023040370
70 VIAL, SINGLE-USE in 1 CARTON (0023-0403-70) / .4 mL in 1 VIAL, SINGLE-USE

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "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": "0023-0403_8fc924b2-2bb1-46ac-845b-41ef1570380e",
  "productndc": "0023-0403",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CARBOXYMETHYLCELLULOSE SODIUM",
  "proprietary_name": "REFRESH PLUS",
  "active_ingred_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "carboxymethylcellulose sodium",
  "start_marketing_date": "19961009",
  "active_numerator_strength": "5"
}

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