Archies Dry Eye Relief

UNIISPL

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

Identification

ManufacturerArchie's Remedies

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
8373700130
30 VIAL, SINGLE-USE in 1 BOX (83737-001-30) / .4 mL in 1 VIAL, SINGLE-USE
ndc11
8373700160
60 VIAL, SINGLE-USE in 1 BOX (83737-001-60) / .4 mL in 1 VIAL, SINGLE-USE

Annotations

UNII (FDA Substance ID)

B697894SGQ

POLYETHYLENE GLYCOL 400

RxCUI 8514

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "B697894SGQ",
    "rxcui": "8514",
    "inchikey": null,
    "display_name": "POLYETHYLENE GLYCOL 400",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "OPHTHALMIC",
  "spl_meta": {
    "07da099b-6b7f-984d-e063-6294a90a12ac": {
      "match": "brand_token",
      "title": "ARCHIES DRY EYE RELIEF (POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL) SOLUTION/ DROPS [ARCHIE'S REMEDIES]",
      "spl_version": "3",
      "published_date": "2026-01-02"
    }
  },
  "productid": "83737-001_474a8539-a4cf-d2de-e063-6394a90aa58b",
  "productndc": "83737-001",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "POLYETHYLENE GLYCOL 400; PROPYLENE GLYCOL",
  "proprietary_name": "Archies Dry Eye Relief",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Polyethylene glycol 400, Propylene glycol",
  "start_marketing_date": "20231016",
  "active_numerator_strength": ".4; .3"
}

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