🇺🇸
United States · US · US:0023-0312_b6d64a52-8a8a-4c90-ac67-41a32cc3c78a
REFRESH LACRI-LUBE
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAllergan, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1100230312041 TUBE in 1 CARTON (0023-0312-04) / 3.5 g in 1 TUBE
- ndc1100230312071 TUBE in 1 CARTON (0023-0312-07) / 7 g in 1 TUBE
Annotations
UNII (FDA Substance ID)
T5L8T28FGP
MINERAL OIL
RxCUI 6972
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "T5L8T28FGP",
"rxcui": "6972",
"inchikey": null,
"display_name": "MINERAL OIL",
"substance_type": "structurallyDiverse",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"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": "0023-0312_b6d64a52-8a8a-4c90-ac67-41a32cc3c78a",
"productndc": "0023-0312",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "MINERAL OIL; PETROLATUM",
"proprietary_name": "REFRESH LACRI-LUBE",
"active_ingred_unit": "mg/g; mg/g",
"application_number": "M018",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "mineral oil, petrolatum",
"start_marketing_date": "19771215",
"active_numerator_strength": "425; 568"
}Related drugs
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