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United States · US · US:69777-250_2d602c5f-384c-b003-e063-6294a90afd2e
OrgaPlus Ultra Pure Sun EX
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBLUEZONWIDE CO.,LTD
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1169777250021 CONTAINER in 1 CARTON (69777-250-02) / 22 g in 1 CONTAINER (69777-250-01)
Annotations
UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4Y5P7MUD51",
"rxcui": "13369",
"inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
"display_name": "OCTINOXATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"d3c422f6-a83d-48fc-94fc-2749666426c8": {
"match": "brand_token",
"title": "ORGAPLUS ULTRA PURE SUN EX 22G (OCTINOXATE, OCTISALATE, OCTOCRYLENE) STICK [BLUEZONWIDE CO.,LTD]",
"spl_version": "2",
"published_date": "2025-02-06"
}
},
"productid": "69777-250_2d602c5f-384c-b003-e063-6294a90afd2e",
"productndc": "69777-250",
"dosage_form": "STICK",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; OCTOCRYLENE",
"proprietary_name": "OrgaPlus Ultra Pure Sun EX",
"active_ingred_unit": "g/22g; g/22g; g/22g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Octinoxate, Octisalate, Octocrylene",
"start_marketing_date": "20180401",
"active_numerator_strength": "1.54; .99; .44"
}Related drugs
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