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United States · US · US:0023-3782_b6ddb19b-f29a-4a65-ac95-33420c2bd4bf
Refresh Relieva PF Xtra
SPLATC A06AG
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeA06AG
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1100233782101 BOTTLE, DROPPER in 1 CARTON (0023-3782-10) / 10 mL in 1 BOTTLE, DROPPER
- ndc1100233782202 BOTTLE, DROPPER in 1 CARTON (0023-3782-20) / 10 mL in 1 BOTTLE, DROPPER
- ndc1100233782351 BOTTLE, DROPPER in 1 CARTON (0023-3782-35) / 10 mL in 1 BOTTLE, DROPPER
- ndc1100233782501 BOTTLE, DROPPER in 1 CARTON (0023-3782-50) / 3.5 mL in 1 BOTTLE, DROPPER
Annotations
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"route": "OPHTHALMIC",
"spl_meta": {
"31bf1d6c-9719-4060-b6a3-409a2fe7b560": {
"match": "brand_token",
"title": "REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.]",
"spl_version": "11",
"published_date": "2026-05-21"
}
},
"productid": "0023-3782_b6ddb19b-f29a-4a65-ac95-33420c2bd4bf",
"productndc": "0023-3782",
"dosage_form": "SOLUTION/ DROPS",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CARBOXYMETHYLCELLULOSE SODIUM; GLYCERIN",
"proprietary_name": "Refresh Relieva PF Xtra",
"active_ingred_unit": "mg/mL; mg/mL",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Carboxymethylcellulose Sodium and Glycerin",
"start_marketing_date": "20240301",
"active_numerator_strength": "5; 9"
}Related drugs
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