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United States · US · US:57619-303_524658a5-3e39-2e46-e063-6294a90a48e3
Splash Tears
UNIISPLATC S01KA
Last synced from FDA National Drug Code directory (United States) on
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 · 2
- ndc1157619303011 BOTTLE, DROPPER in 1 CARTON (57619-303-01) / 15 mL in 1 BOTTLE, DROPPER
- ndc1157619303031 BOTTLE, DROPPER in 1 CARTON (57619-303-03) / 2 mL in 1 BOTTLE, DROPPER
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": "57619-303_524658a5-3e39-2e46-e063-6294a90a48e3",
"productndc": "57619-303",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "HYPROMELLOSE 2910 (4000 MPA.S)",
"proprietary_name": "Splash Tears",
"active_ingred_unit": "g/100mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Hypromellose",
"start_marketing_date": "20200513",
"active_numerator_strength": ".2"
}Related drugs
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