Dry Eye Relief

UNIISPL

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

Identification

ManufacturerCARDINAL HEALTH 110, LLC. DBA LEADER

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7000000891
1 BOTTLE, DROPPER in 1 CARTON (70000-0089-1) / 15 mL in 1 BOTTLE, DROPPER

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": {
    "0397507d-4b6e-c679-e063-6294a90a0b33": {
      "match": "brand_token",
      "title": "DRY SKIN HEALING (PETROLATUM) LOTION [WALGREEN]",
      "spl_version": "6",
      "published_date": "2026-05-11"
    }
  },
  "productid": "70000-0089_b2fd3f1c-69bb-4c0c-9a11-1c135377045c",
  "productndc": "70000-0089",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED",
  "proprietary_name": "Dry Eye Relief",
  "active_ingred_unit": "mg/mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Carboxymethylcellulose sodium",
  "start_marketing_date": "20210309",
  "active_numerator_strength": "10"
}

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