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United States · US · US:55910-589_514e49e7-49a0-cc3d-e063-6294a90ac679
Ultra
UNIISPLATC D08AE05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerOld East Main Co.
CountryUS (United States)
ATC codeD08AE05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1155910589381124 mL in 1 BOTTLE, DISPENSING (55910-589-38)
- ndc115591058944532 mL in 1 BOTTLE, DISPENSING (55910-589-44)
Annotations
UNII (FDA Substance ID)
0F32U78V2Q
CHLOROXYLENOL
RxCUI 20877
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "0F32U78V2Q",
"rxcui": "20877",
"inchikey": "OSDLLIBGSJNGJE-UHFFFAOYSA-N",
"display_name": "CHLOROXYLENOL",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"52d4b1c1-7431-4f8c-e063-6294a90ad482": {
"match": "brand_token",
"title": "ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN BROAD SPECTRUM SPF 40 (ZINC OXIDE) CREAM [GRACE AND FIRE USA INC.]",
"spl_version": "1",
"published_date": "2026-05-29"
}
},
"productid": "55910-589_514e49e7-49a0-cc3d-e063-6294a90ac679",
"productndc": "55910-589",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CHLOROXYLENOL",
"proprietary_name": "Ultra",
"active_ingred_unit": "mg/mL",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Chloroxylenol 0.3%",
"start_marketing_date": "20170117",
"active_numerator_strength": "3"
}Related drugs
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