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United States · US · US:76354-120_43961b71-929a-943b-e063-6294a90afd73
Naturium Sulfur Spot Treatment 8%
UNIISPLATC D10AB02
Last synced from FDA National Drug Code directory (United States) on
Identification
Manufacturere.l.f. Cosmetics, Inc
CountryUS (United States)
ATC codeD10AB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1176354120011 TUBE in 1 CARTON (76354-120-01) / 15 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": {
"1c3489a6-5b98-2dc2-e063-6294a90a0695": {
"match": "brand_token",
"title": "NATURIUM DEW GLOW TINTED MOISTURIZER SPF50-DEEP (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION NATURIUM DEW GLOW TINTED MOISTURIZER SPF50-MEDIUM (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION NATURIUM DEW GLOW TINTED MOISTURIZER SPF50-LIGHT (HOMOSALATE, OCTISALATE, AVOBENZONE) LOTION [PML NYC, LLC]",
"spl_version": "5",
"published_date": "2026-04-17"
}
},
"productid": "76354-120_43961b71-929a-943b-e063-6294a90afd73",
"productndc": "76354-120",
"dosage_form": "LIQUID",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SULFUR",
"proprietary_name": "Naturium Sulfur Spot Treatment 8%",
"active_ingred_unit": "mg/mL",
"application_number": "M006",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sulfur",
"start_marketing_date": "20220617",
"active_numerator_strength": "80"
}Related drugs
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