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United States · US · US:58466-108_f1bea67c-e6e1-44cf-b088-53a00d157b70
celazome
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDermazone LLC
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1158466108041 BOTTLE, DISPENSING in 1 CARTON (58466-108-04) / 113 g in 1 BOTTLE, DISPENSING
Annotations
UNII (FDA Substance ID)
V06SV4M95S
HOMOSALATE
RxCUI 91326
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "V06SV4M95S",
"rxcui": "91326",
"inchikey": "WSSJONWNBBTCMG-UHFFFAOYSA-N",
"display_name": "HOMOSALATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"99fb90ca-6527-459b-8af2-627ea9abe11b": {
"match": "brand_token",
"title": "CELAZOME MOISTURIZING SPF 29 ACTIVE WITH DNARESCUE (OXYBENZONE, OCTINOXATE, OCTISALATE, AND HOMOSALATE) CREAM [DERMAZONE LLC]",
"spl_version": "3",
"published_date": "2025-07-28"
}
},
"productid": "58466-108_f1bea67c-e6e1-44cf-b088-53a00d157b70",
"productndc": "58466-108",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE",
"proprietary_name": "celazome",
"active_ingred_unit": "mg/g; mg/g; mg/g; mg/g",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "OXYBENZONE, OCTINOXATE, OCTISALATE, and HOMOSALATE",
"start_marketing_date": "20151001",
"active_numerator_strength": "50; 75; 50; 60"
}Related drugs
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