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United States · US · US:11673-771_4202718c-a8c4-9344-e063-6394a90ace0f
Up and Up Dry Eye Relief Lubricant Eye Drops
SPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerTarget Corporation
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1111673771012 BOTTLE, DROPPER in 1 BOX (11673-771-01) / 15 mL in 1 BOTTLE, DROPPER
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "OPHTHALMIC",
"spl_meta": {
"51c0a953-93cb-4d0a-b51c-02d9482d1746": {
"match": "brand_token",
"title": "UP AND UP ALLERGY RELIEF NASAL (FLUTICASONE PROPIONATE) SPRAY, METERED [TARGET CORPORATION]",
"spl_version": "12",
"published_date": "2026-05-13"
}
},
"productid": "11673-771_4202718c-a8c4-9344-e063-6394a90ace0f",
"productndc": "11673-771",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CARBOXYMETHYLCELLULOSE SODIUM",
"proprietary_name": "Up and Up Dry Eye Relief Lubricant Eye Drops",
"active_ingred_unit": "mg/mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Carboxymethylcellulose Sodium",
"start_marketing_date": "20251031",
"active_numerator_strength": "5"
}Access this data programmatically
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