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United States Β· US Β· US:84938-001_47373d02-07ae-7104-e063-6294a90a0265

EYE DROPS

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerFoshan Sugar Max Cosmetics CO.,Ltd
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 1

  • ndc11
    8493800101
    2 BOTTLE in 1 BOX (84938-001-01) / 15 mL in 1 BOTTLE

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": {
    "52c62397-58f1-d34d-e063-6294a90a6faf": {
      "match": "brand_token",
      "title": "EYE ITCH RELIEF (KETOTIFEN FUMARATE) SOLUTION [REDPHARM DRUG]",
      "spl_version": "1",
      "published_date": "2026-05-28"
    }
  },
  "productid": "84938-001_47373d02-07ae-7104-e063-6294a90a0265",
  "productndc": "84938-001",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED",
  "proprietary_name": "EYE DROPS",
  "active_ingred_unit": "g/100mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Carboxymethylcellulose sodium",
  "start_marketing_date": "20251231",
  "active_numerator_strength": ".25"
}

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EYE DROPS (US) β€” Drug Database