Splash Redness Reliever

UNIISPLATC S01KA

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

Identification

ManufacturerLABORATORIOS SOPHIA, S.A. DE C.V.

CountryUS (United States)

ATC codeS01KA

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5761930401
1 BOTTLE, PLASTIC in 1 CARTON (57619-304-01) / 15 mL in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)

RN3152OP35

HYPROMELLOSE 2910 (4000 MPA.S)

RxCUI 1300455

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "RN3152OP35",
    "rxcui": "1300455",
    "inchikey": null,
    "display_name": "HYPROMELLOSE 2910 (4000 MPA.S)",
    "substance_type": "polymer",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "OPHTHALMIC",
  "spl_meta": {
    "a58a8478-9cc5-aa39-e053-2995a90a347d": {
      "match": "brand_token",
      "title": "SPLASH TEARS (HYPROMELLOSE) SOLUTION/ DROPS [LABORATORIOS SOPHIA, S.A. DE C.V.]",
      "spl_version": "10",
      "published_date": "2026-06-01"
    }
  },
  "productid": "57619-304_351e11b7-7c46-9bc7-e063-6294a90a46a7",
  "productndc": "57619-304",
  "dosage_form": "SOLUTION/ DROPS",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYPROMELLOSE 2910 (4000 MPA.S); NAPHAZOLINE HYDROCHLORIDE",
  "proprietary_name": "Splash Redness Reliever",
  "active_ingred_unit": "g/100mL; g/100mL",
  "application_number": "M018",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Hypromellose, Naphazoline hydrochloride",
  "start_marketing_date": "20230425",
  "active_numerator_strength": ".2; .02"
}

Related drugs

Other records sharing ATC code S01KA.

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