🇺🇸
United States · US · US:45802-040_88f77de3-64b1-4ef8-9b6f-39c54ba9f9e4
SELENIUM SULFIDE
Orange BookUNIISPLATC D01AE13
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPadagis Israel Pharmaceuticals Ltd
CountryUS (United States)
ATC codeD01AE13
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc114580204064118 mL in 1 BOTTLE (45802-040-64)
Annotations
UNII (FDA Substance ID)
Z69D9E381Q
SELENIUM SULFIDE
RxCUI 36345
Orange Book
A089996
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "Z69D9E381Q",
"rxcui": "36345",
"inchikey": "JNMWHTHYDQTDQZ-UHFFFAOYSA-N",
"display_name": "SELENIUM SULFIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"1c2cc0ad-f859-470b-be4b-f98e010a2e5c": {
"match": "brand_token",
"title": "SELENIUM COMBINATION 9245 (SELENIUM COMBINATION) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]",
"spl_version": "2",
"published_date": "2026-01-12"
}
},
"productid": "45802-040_88f77de3-64b1-4ef8-9b6f-39c54ba9f9e4",
"productndc": "45802-040",
"dosage_form": "LOTION",
"orange_book": {
"appl_no": "089996",
"products": [
{
"rs": true,
"rld": false,
"te_code": null,
"strength": "2.5%",
"product_no": "001",
"approval_date": "Jan 10, 1991"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SELENIUM SULFIDE",
"proprietary_name": "SELENIUM SULFIDE",
"active_ingred_unit": "mg/100mL",
"application_number": "ANDA089996",
"marketing_category": "ANDA",
"nonproprietary_name": "SELENIUM SULFIDE",
"start_marketing_date": "20060925",
"active_numerator_strength": "2.5"
}Related drugs
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