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United States · US · US:42281-001_2cdcb7de-ce78-3d94-e063-6394a90a8bec
Belli Acne Control Spot Treatment
UNIISPLATC D10AB02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerBODY HALO LLC
CountryUS (United States)
ATC codeD10AB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1142281001001 TUBE in 1 CARTON (42281-001-00) / 14.75 mL in 1 TUBE
Annotations
UNII (FDA Substance ID)
70FD1KFU70
SULFUR
RxCUI 10223
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "70FD1KFU70",
"rxcui": "10223",
"inchikey": "JLQNHALFVCURHW-UHFFFAOYSA-N",
"display_name": "SULFUR",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"da979b69-1e4c-4e2b-82c3-0f155e978652": {
"match": "brand_token",
"title": "BELLI ACNE CONTROL SPOT TREATMENT (SULFUR) CREAM [BODY HALO LLC]",
"spl_version": "8",
"published_date": "2025-01-30"
}
},
"productid": "42281-001_2cdcb7de-ce78-3d94-e063-6394a90a8bec",
"productndc": "42281-001",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SULFUR",
"proprietary_name": "Belli Acne Control Spot Treatment",
"active_ingred_unit": "mg/mL",
"application_number": "M006",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "SULFUR",
"start_marketing_date": "20120102",
"active_numerator_strength": "30"
}Related drugs
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